Thursday, September 29, 2016

Salicylates


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Salicylates are nonsteroidal anti-inflammatory drugs. They inhibit the synthesis of prostaglandin and other mediators in the process of inflammation and have anti-inflammatory, antipyretic and analgesic properties. Salicylates can be used to reduce fever, pain and inflammation such as in arthritis.

See also

Medical conditions associated with salicylates:

  • Angina
  • Angina Pectoris Prophylaxis
  • Ankylosing Spondylitis
  • Antiphospholipid Syndrome
  • Aseptic Necrosis
  • Back Pain
  • Fever
  • Gas
  • Headache
  • Heart Attack
  • Indigestion
  • Inflammatory Conditions
  • Ischemic Stroke
  • Ischemic Stroke, Prophylaxis
  • Juvenile Rheumatoid Arthritis
  • Kawasaki Disease
  • Myocardial Infarction, Prophylaxis
  • Niacin Flush
  • Osteoarthritis
  • Pain
  • Prevention of Thromboembolism in Atrial Fibrillation
  • Prosthetic Heart Valves
  • Prosthetic Heart Valves, Mechanical Valves
  • Revascularization Procedures, Prophylaxis
  • Rheumatic Fever
  • Rheumatoid Arthritis
  • Sciatica
  • Systemic Lupus Erythematosus
  • Thromboembolic Stroke Prophylaxis
  • Transient Ischemic Attack

Drug List:

First generation cephalosporins


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Cephalosporins are a group of broad spectrum, semi-synthetic beta-lactam antibiotics derived from the mould Cephalosporium. They are divided into three groups: Cephalosporin N and C are chemically related to penicillins and Cephalosporin P a steroid antibiotic resembles fusidic acid.


The mechanism of action of cephalosporins is the same as penicillins. They interfere with bacterial cell wall synthesis.


Semisynthetic broad-spectrum cephalosporins have been produced by the addition of different side chains, to the Cephalosporin C nucleus.


They are classified according to the chronological order in which they were produced.


First generation Cephalosporins, were the first lot of this class of antibiotics that were produced.

See also

Medical conditions associated with first generation cephalosporins:

  • Acne
  • Bacterial Endocarditis Prevention
  • Bacterial Infection
  • Bladder Infection
  • Bone infection
  • Cholecystitis
  • Endocarditis
  • Impetigo
  • Joint Infection
  • Kidney Infections
  • Otitis Media
  • Peritonitis
  • Pharyngitis
  • Pneumonia
  • Prevention of Perinatal Group B Streptococcal Disease
  • Prostatitis
  • Septicemia
  • Skin and Structure Infection
  • Skin Infection
  • Surgical Prophylaxis
  • Tonsillitis/Pharyngitis
  • Upper Respiratory Tract Infection
  • Urinary Tract Infection

Drug List:

Mondus




Mondus may be available in the countries listed below.


Ingredient matches for Mondus



Flunarizine

Flunarizine dihydrochloride (a derivative of Flunarizine) is reported as an ingredient of Mondus in the following countries:


  • Argentina

International Drug Name Search

Quinolones


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Quinolones are synthetic, bactericidal antibacterial agents with broad-spectrum activity. They inhibit the enzyme topoisomerase II, a DNA gyrase that is necessary for the replication of the microorganism. Topoisomerase II enzyme produces a negative supercoil on DNA, permitting transcription or replication so by inhibiting this enzyme DNA replication and transcription is blocked.

See also

Medical conditions associated with quinolones:

  • Anthrax
  • Anthrax Prophylaxis
  • Bacteremia
  • Bacterial Infection
  • Bladder Infection
  • Bone infection
  • Bronchitis
  • Campylobacter Gastroenteritis
  • Cervicitis
  • Chancroid
  • Chlamydia Infection
  • Cholera
  • Crohn's Disease
  • Cutaneous Bacillus anthracis
  • Diverticulitis
  • Epididymitis, Non-Specific
  • Epididymitis, Sexually Transmitted
  • Febrile Neutropenia
  • Gonococcal Infection, Disseminated
  • Gonococcal Infection, Uncomplicated
  • Granuloma Inguinale
  • Infection Prophylaxis
  • Infectious Diarrhea
  • Intraabdominal Infection
  • Joint Infection
  • Kidney Infections
  • Leprosy, Borderline
  • Leprosy, Lepromatous
  • Meningococcal Meningitis Prophylaxis
  • Methicillin-Resistant Staphylococcus Aureus Infection
  • Mycobacterium avium-intracellulare, Treatment
  • Nongonococcal Urethritis
  • Nosocomial Pneumonia
  • Otitis Media
  • Pelvic Infections
  • Pelvic Inflammatory Disease
  • Peritonitis
  • Plague
  • Pneumonia
  • Pneumonia with Cystic Fibrosis
  • Prevention of Bladder infection
  • Prostatitis
  • Rabbit Fever
  • Salmonella Enteric Fever
  • Salmonella Gastroenteritis
  • Shigellosis
  • Sinusitis
  • Skin and Structure Infection
  • Skin Infection
  • Small Bowel Bacterial Overgrowth
  • Strep Throat
  • Streptococcal Infection
  • Transurethral Prostatectomy
  • Traveler's Diarrhea
  • Tuberculosis, Active
  • Typhoid Fever
  • Urinary Tract Infection

Drug List:

Loop diuretics


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Loop diuretics inhibit the Na+/K+/2Cl- co-transporter in the thick ascending loop of Henle, in the kidneys and stop the transport of sodium chloride out of the tubule into the interstitial tissue, causing a decrease in sodium and chloride re-absorption. They act on the chloride-binding site and have a direct inhibiting effect on the carrier.


Inhibition of this transporter leads to a significant increase in concentration of ions in the tubule and reduced hypertonicity in the surrounding interstitium, causing less water to be reabsorbed into the blood. This causes more urine to be produced and a decrease in blood volume.

See also

Medical conditions associated with loop diuretics:

  • Ascites
  • Edema
  • Heart Failure
  • High Blood Pressure
  • Hypercalcemia
  • Nonobstructive Oliguria
  • Oliguria
  • Pulmonary Edema
  • Renal Failure
  • Renal Transplant

Drug List:

B-Tablock




B-Tablock may be available in the countries listed below.


Ingredient matches for B-Tablock



Levobunolol

Levobunolol hydrochloride (a derivative of Levobunolol) is reported as an ingredient of B-Tablock in the following countries:


  • Brazil

International Drug Name Search

Lung surfactants


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Lung surfactants are made from animal lung extract and contain phospholipids. Natural surfactant is produced by the alveolar cells in the lungs and line mainly the alveoli and small bronchioles, and prevents the alveoli from collapsing. Lung surfactant makes it easier for oxygen to penetrate the lung surface lining and move into the blood. Without the lung surfactant it would be extremely hard to breathe, and transfer of oxygen through the surface that lines the lungs would be very difficult.


Natural surfactant is produced by the fetus before they are born and their lungs are prepared to breathe properly by about 37 week gestation. In unexpected circumstances where labor starts early or a pre-term emergency caesarean is performed, lung surfactant is given intratracheally to the premature infant to prevent respiratory distress syndrome.

See also

Medical conditions associated with lung surfactants:

  • Respiratory Distress Syndrome

Drug List:

Tridione


Tridione is a brand name of trimethadione, approved by the FDA in the following formulation(s):


TRIDIONE (trimethadione - tablet; oral)



  • Manufacturer: ABBOTT

    Approved Prior to Jan 1, 1982

    Strength(s): 150MG [RLD]

Has a generic version of Tridione been approved?


No. There is currently no therapeutically equivalent version of Tridione available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Tridione. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents

There are no current U.S. patents associated with Tridione.

See also...

  • Tridione Consumer Information (Cerner Multum)
  • Trimethadione Consumer Information (Cerner Multum)

Erytab




Erytab may be available in the countries listed below.


Ingredient matches for Erytab



Erythromycin

Erythromycin stearate (a derivative of Erythromycin) is reported as an ingredient of Erytab in the following countries:


  • Sri Lanka

International Drug Name Search

Kinrix


Generic Name: diphtheria, pertussis acellular, tetanus, and polio (dif THEER ee a, per TUS is a SEL yoo lar, TET a nus, POE lee oh)

Brand Names: Kinrix


What is diphtheria, pertussis acellular, tetanus, and polio vaccine?

Diphtheria, pertussis acellular, tetanus, and polio are serious diseases caused by bacteria.


Diphtheria causes a thick coating in the nose, throat, and airway. It can lead to breathing problems, paralysis, heart failure, or death.


Pertussis (whooping cough) causes coughing so severe that it interferes with eating, drinking, or breathing. These spells can last for weeks and can lead to pneumonia, seizures (convulsions), brain damage, and death.


Tetanus (lockjaw) causes painful tightening of the muscles, usually all over the body. It can lead to "locking" of the jaw so the victim cannot open the mouth or swallow. Tetanus leads to death in about 1 out of 10 cases.


Polio affects the central nervous system and spinal cord. It can cause muscle weakness and paralysis. Polio is a life-threatening condition because it can paralyze the muscles that help you breathe.


Diphtheria, pertussis, and polio are spread from person to person. Tetanus enters the body through a cut or wound.


The diphtheria, pertussis acellular, tetanus, and polio vaccine is used to help prevent these diseases in children who are ages 4 through 6 years (before the 7th birthday) who have received prior vaccination with a DTaP and IPV series.


This vaccine works by exposing your child to a small dose of the bacteria or a protein from the bacteria, which causes the body to develop immunity to the disease. This vaccine will not treat an active infection that has already developed in the body.


Like any vaccine, the diphtheria, pertussis acellular, tetanus, and polio vaccine may not provide protection from disease in every person.


What is the most important information I should know about this vaccine?


The diphtheria, pertussis acellular, tetanus, and polio vaccine is given as the 5th dose in a series of DTaP immunizations and the 4th dose in a series of IPV immunizations. The shot is usually given to a child who is at least 4 years old or has not yet reached his or her 7th birthday. Your child's individual dose schedule may be different from these guidelines. Follow your doctor's instructions or the schedule recommended by the health department of the state you live in.


Be sure your child receives all recommended doses in the DTaP and IPV series. If your child does not receive the full series of vaccines, he or she may not be fully protected against the disease.


Your child can still receive a vaccine if he or she has a cold or fever. In the case of a more severe illness with a fever or any type of infection, wait until the child gets better before receiving this vaccine.


Your child should not receive this vaccine if he or she had a life-threatening allergic reaction to a vaccine containing diphtheria, pertussis, tetanus, or polio.

Keep track of any and all side effects your child has after receiving this vaccine. If the child ever needs to receive a booster dose, you will need to tell the doctor if the previous shots caused any side effects.


Becoming infected with diphtheria, pertussis, tetanus, or polio is much more dangerous to your child's health than receiving the vaccine to protect against these diseases. Like any medicine, this vaccine can cause side effects, but the risk of serious side effects is extremely low.


What should I discuss with my healthcare provider before receiving this vaccine?


Your child should not receive this vaccine if he or she had a life-threatening allergic reaction to a vaccine containing diphtheria, pertussis, tetanus, or polio. Your child should not receive this vaccine if the child has had a decreased level of consciousness within the past 7 days, or if the child has a neurologic disorder or disease affecting the brain.

Your child may not be able to receive this vaccine if he or she has ever received a similar vaccine that caused any of the following within 48 hours:



  • a very high fever (over 104 degrees);




  • excessive crying for 3 hours or longer;




  • fainting or going into shock;




  • seizure (convulsions); or




  • Guillain-Barré syndrome (within 6 weeks after receiving a vaccine containing tetanus).



Before receiving this vaccine, tell the doctor if your child has:



  • a history of seizures;




  • an allergy to latex rubber;




  • if the child is using steroid medication or receiving cancer chemotherapy or radiation treatment; or




  • a weak immune system caused by disease, bone marrow transplant, or by using certain medicines or receiving cancer treatments.



Your child can still receive a vaccine if he or she has a cold or fever. In the case of a more severe illness with a fever or any type of infection, wait until the child gets better before receiving this vaccine.


How is this vaccine given?


This vaccine is given as an injection into a muscle. Your child will receive this injection in a doctor's office or other clinic setting.


The diphtheria, pertussis acellular, tetanus, and polio vaccine is given as the 5th dose in a series of DTaP immunizations and the 4th dose in a series of IPV immunizations. The shot is usually given to a child who is at least 4 years old or has not yet reached his or her 7th birthday. Your child's individual dose schedule may be different from these guidelines. Follow your doctor's instructions or the schedule recommended by the health department of the state you live in.


Your doctor may recommend treating fever and pain with an aspirin-free pain reliever such as acetaminophen (Tylenol) or ibuprofen (Motrin, Advil, and others) when the shot is given and for the next 24 hours. Follow the label directions or your doctor's instructions about how much of this medicine to give your child.


It is especially important to prevent fever from occurring in a child who has a seizure disorder such as epilepsy.

What happens if I miss a dose?


Contact your doctor if you will miss a booster dose or if you get behind schedule. The next dose should be given as soon as possible. There is no need to start over.


Be sure your child receives all recommended doses in the DTaP and IPV series. If your child does not receive the full series of vaccines, he or she may not be fully protected against the disease.


What happens if I overdose?


An overdose of this vaccine is unlikely to occur.


What should I avoid before or after receiving this vaccine?


Follow your doctor's instructions about any restrictions on food, beverages, or activity after receiving the vaccine.


This vaccine side effects


Your child should not receive a booster vaccine if he or she had a life-threatening allergic reaction after the first shot.

Keep track of any and all side effects your child has after receiving this vaccine. If the child ever needs to receive a booster dose, you will need to tell the doctor if the previous shots caused any side effects.


Becoming infected with diphtheria, pertussis, tetanus, or polio is much more dangerous to your child's health than receiving the vaccine to protect against these diseases. Like any medicine, this vaccine can cause side effects, but the risk of serious side effects is extremely low.


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if the child has any of these serious side effects:



  • extreme drowsiness, fainting;




  • fussiness, irritability, crying for an hour or longer;




  • seizure (black-out or convulsions); or




  • high fever.



Less serious side effects may include:



  • redness, pain, tenderness, or swelling where the shot was given;




  • drowsiness;




  • mild fussiness or crying;




  • low fever; or




  • loss of appetite.



This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect diphtheria, pertussis acellular, tetanus, and polio vaccine?


Before receiving this vaccine, tell the doctor about all other vaccines your child has recently received.

Also tell the doctor if your child has received drugs or treatments in the past 2 weeks that can weaken the immune system, including:



  • an oral, nasal, inhaled, or injectable steroid medicine;




  • medications to treat psoriasis, rheumatoid arthritis, or other autoimmune disorders, such as azathioprine (Imuran), efalizumab (Raptiva), etanercept (Enbrel), leflunomide (Arava), and others; or




  • medicines to treat or prevent organ transplant rejection, such as basiliximab (Simulect), cyclosporine (Sandimmune, Neoral, Gengraf), muromonab-CD3 (Orthoclone), mycophenolate mofetil (CellCept), sirolimus (Rapamune), or tacrolimus (Prograf).



If your child is using any of these drugs, this vaccine may not work as well.


This list is not complete and there may be other drugs that can affect this vaccine. Tell your doctor about all the prescription and over-the-counter medications your child has received. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your child's doctor.



More Kinrix resources


  • Kinrix Side Effects (in more detail)
  • Kinrix Use in Pregnancy & Breastfeeding
  • Kinrix Drug Interactions
  • Kinrix Support Group
  • 0 Reviews for Kinrix - Add your own review/rating


  • Kinrix Prescribing Information (FDA)

  • Kinrix Advanced Consumer (Micromedex) - Includes Dosage Information

  • Kinrix MedFacts Consumer Leaflet (Wolters Kluwer)

  • Kinrix Consumer Overview



Compare Kinrix with other medications


  • Diphtheria Prophylaxis
  • Pertussis Prophylaxis
  • Poliomyelitis Prophylaxis
  • Tetanus Prophylaxis


Where can I get more information?


  • Your doctor or pharmacist may have information about this vaccine written for health professionals that you may read. You may also find additional information from your local health department or the Centers for Disease Control and Prevention.

See also: Kinrix side effects (in more detail)


Chymase




Chymase may be available in the countries listed below.


Ingredient matches for Chymase



Chymotrypsin

Chymotrypsin is reported as an ingredient of Chymase in the following countries:


  • Taiwan

International Drug Name Search

Peripherally acting antiobesity agents


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Peripherally acting antiobesity agents are drugs that assist with weight loss, without affecting the brain or suppressing the appetite. It inhibits pancreatic lipase and prevents fat breakdown in the gastrointestinal tract therefore reduces intestinal absorption of fat. It is used to treat obesity, with diet and exercise.

See also

Medical conditions associated with peripherally acting antiobesity agents:

  • Nonalcoholic Fatty Liver Disease
  • Obesity

Drug List:

Growth hormone receptor blockers


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Growth hormone receptor blockers are drugs that bind to the growth hormone receptor and make it non-functional. As a result growth hormone cannot exert its effect. These agents are used to control acromegaly.

See also

Medical conditions associated with growth hormone receptor blockers:

  • Acromegaly

Drug List:

Synvomin




Synvomin may be available in the countries listed below.


Ingredient matches for Synvomin



Promethazine

Promethazine teoclate (a derivative of Promethazine) is reported as an ingredient of Synvomin in the following countries:


  • Hong Kong

International Drug Name Search

Group IV antiarrhythmics


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

See also

Medical conditions associated with group IV antiarrhythmics:

  • Angina
  • Angina Pectoris Prophylaxis
  • Arrhythmia
  • Atrial Fibrillation
  • Atrial Flutter
  • Bipolar Disorder
  • Cluster Headaches
  • Heart Failure
  • High Blood Pressure
  • Idiopathic Hypertrophic Subaortic Stenosis
  • Migraine Prevention
  • Nocturnal Leg Cramps
  • Raynaud's Syndrome
  • Supraventricular Tachycardia

Drug List:

Oyster Shell Calcium with Vitamin D


Generic Name: calcium and vitamin D combination (KAL see um and VYE ta min D)

Brand Names: Calcarb with D, Calcet, Calcio Del Mar, Calcitrate with D, Calcium 600+D, Caltrate 600 with D, Caltrate 600 with D Plus Soy, Caltrate Colon Health, Citracal + D, Citracal 250 mg + D, Citracal Creamy Bites, Citracal Maximum + D, Citracal Petites, Citrus Calcium with Vitamin D, Dical-D, Os-Cal 250 with D, Os-Cal 500 + D, Os-Cal with D, Oysco 500 with D, Oysco D, Oyst-Cal-D, Oyster Shell Calcium with Vitamin D, Oyster-D, Oystercal-D, Posture-D H/P, Risacal-D


What is Oyster Shell Calcium with Vitamin D (calcium and vitamin D combination)?

Calcium is a mineral that is found naturally in foods. Calcium is necessary for many normal functions of your body, especially bone formation and maintenance.


Vitamin D is important for the absorption of calcium from the stomach and for the functioning of calcium in the body.


Calcium and vitamin D combination is used to prevent or to treat a calcium deficiency.


Calcium and vitamin D combination may also be used for other purposes not listed in this medication guide.


What is the most important information I should know about Oyster Shell Calcium with Vitamin D (calcium and vitamin D combination)?


Before you take calcium and vitamin D combination, tell your doctor if you have kidney disease, past or present kidney stones, heart disease, circulation problems, a parathyroid disorder, or if you are pregnant or breast-feeding.


Avoid taking any other vitamin or mineral supplements that contain calcium or vitamin D without first talking to your doctor.

Before taking calcium and vitamin D combination, tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.


What should I tell my healthcare provider before taking Oyster Shell Calcium with Vitamin D (calcium and vitamin D combination)?


If you have certain conditions, you may need a dose adjustment or special tests to safely use this medication. Before you take calcium and vitamin D combination, tell your doctor if you have:


  • kidney disease;

  • past or present kidney stones;


  • heart disease;




  • circulation problems; or




  • a parathyroid gland disorder.




Talk to your doctor before taking calcium and vitamin D combination if you are pregnant. Talk to your doctor before taking calcium and vitamin D combination if you are breast-feeding.

How should I take Oyster Shell Calcium with Vitamin D (calcium and vitamin D combination)?


Take this medication exactly as prescribed by your doctor. Do not take it in larger amounts or for longer than recommended. Follow the directions on your prescription label.


Take the calcium and vitamin D regular tablet with a full glass of water.

The chewable tablet should be chewed before you swallow it.


Store calcium and vitamin D combination at room temperature away from moisture and heat.

What happens if I miss a dose?


Take the missed dose as soon as you remember. If it is almost time for your next dose, wait until then to take the medicine and skip the missed dose. Do not take extra medicine to make up the missed dose.


What happens if I overdose?


Seek emergency medical attention if you think you have used too much of this medicine.

Overdose symptoms may include irregular heartbeat, stomach pain, nausea, vomiting, dry mouth, a metallic taste in your mouth, confusion, loss of appetite, constipation, weakness, headache, confusion, or fainting.


What should I avoid while taking Oyster Shell Calcium with Vitamin D (calcium and vitamin D combination)?


Avoid taking any other vitamin or mineral supplements that contain calcium or vitamin D without first talking to your doctor.

Oyster Shell Calcium with Vitamin D (calcium and vitamin D combination) side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Less serious side effects may include:



  • an irregular heartbeat;




  • nausea, vomiting, or decreased appetite;




  • dry mouth;




  • constipation;




  • weakness;




  • headache;




  • a metallic taste;




  • muscle or bone pain; or




  • drowsiness.



This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect Oyster Shell Calcium with Vitamin D (calcium and vitamin D combination)?


Before taking calcium and vitamin D combination, tell your doctor if you are taking:



  • digoxin (Lanoxin, Lanoxicaps);




  • antacids containing calcium, aluminum, or magnesium;




  • other calcium supplements;




  • calcitriol (Rocaltrol) or other vitamin D supplements; or




  • a tetracycline antibiotic such as demeclocycline (Declomycin), doxycycline (Adoxa, Doryx, Oracea, Vibramycin), minocycline (Dynacin, Minocin, Solodyn, Vectrin), or tetracycline (Brodspec, Panmycin, Sumycin, Tetracap).



This list is not complete and there may be other drugs that can interact with calcium and vitamin D combination. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.



More Oyster Shell Calcium with Vitamin D resources


  • Oyster Shell Calcium with Vitamin D Use in Pregnancy & Breastfeeding
  • Oyster Shell Calcium with Vitamin D Drug Interactions
  • 0 Reviews for Oyster Shell Calcium with Vitamin D - Add your own review/rating


Compare Oyster Shell Calcium with Vitamin D with other medications


  • Dietary Supplementation
  • Osteoporosis


Where can I get more information?


  • Your pharmacist can provide more information about calcium and vitamin D combination.


Glycoprotein platelet inhibitors


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Glycoprotein platelet inhibitors prevent platelet adhesion by binding to the glycoprotein IIb/IIIa receptors on the plasma membrane of platelets. They stop the actual substrates of the glycoprotein receptors from binding to the receptor, so inhibit platelets from sticking together to form a thrombus, which can lead to stroke, myocardial infarction or deep vein thrombosis.


Glycoprotein platelet inhibitors are used in patients with angina, after a heart attack, angioplasty or other types of coronary vasculature procedures.

See also

Medical conditions associated with glycoprotein platelet inhibitors:

  • Acute Coronary Syndrome
  • Angina
  • Heart Attack
  • High Risk Percutaneous Transluminal Angioplasty
  • Percutaneous Coronary Intervention

Drug List:

Effontil




Effontil may be available in the countries listed below.


Ingredient matches for Effontil



Etilefrine

Etilefrine hydrochloride (a derivative of Etilefrine) is reported as an ingredient of Effontil in the following countries:


  • Venezuela

International Drug Name Search

Carbo Medicinalis Sanova




Carbo Medicinalis Sanova may be available in the countries listed below.


Ingredient matches for Carbo Medicinalis Sanova



Charcoal

Charcoal, Activated is reported as an ingredient of Carbo Medicinalis Sanova in the following countries:


  • Austria

International Drug Name Search

Vaccine combinations


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

See also

Medical conditions associated with vaccine combinations:

  • Diphtheria Prophylaxis
  • Haemophilus influenzae Prophylaxis
  • Hepatitis A Prophylaxis
  • Hepatitis B Prevention
  • Measles Prophylaxis
  • Mumps Prophylaxis
  • Pertussis Prophylaxis
  • Poliomyelitis Prophylaxis
  • Rubella Prophylaxis
  • Tetanus
  • Tetanus Prophylaxis
  • Varicella-Zoster, Prophylaxis

Drug List:

Oberdol




Oberdol may be available in the countries listed below.


Ingredient matches for Oberdol



Ibuprofen

Ibuprofen is reported as an ingredient of Oberdol in the following countries:


  • Spain

International Drug Name Search

Elo




Elo may be available in the countries listed below.


Ingredient matches for Elo



Loratadine

Loratadine is reported as an ingredient of Elo in the following countries:


  • Bangladesh

International Drug Name Search

Minipress


Generic Name: prazosin (PRA zoe sin)

Brand Names: Minipress


What is Minipress (prazosin)?

Prazosin is in a group of drugs called alpha-adrenergic (AL-fa ad-ren-ER-jik) blockers. Prazosin relaxes your veins and arteries so that blood can more easily pass through them.


Prazosin is used to treat hypertension (high blood pressure).


Prazosin may also be used for other purposes not listed in this medication guide.


What is the most important information I should know about Minipress (prazosin)?


You should not use this medication if you are allergic to prazosin or similar medicines such as alfuzosin (Uroxatral), doxazosin (Cardura), silodosin (Rapaflo), tamsulosin (Flomax), or terazosin (Hytrin). Prazosin may cause dizziness or fainting, especially when you first start taking it or whenever your dose is changed. Be careful if you drive or do anything that requires you to be alert. Avoid standing for long periods of time or becoming overheated during exercise and in hot weather. Avoid getting up too fast from a sitting or lying position, or you may feel dizzy.

Prazosin can affect your pupils during cataract surgery. Tell your eye surgeon ahead of time that you are using this medication. Do not stop using prazosin before surgery unless your surgeon tells you to.


Tell your doctor about all other medications you use, especially other blood pressure medications including diuretics (water pills).


What should I discuss with my healthcare provider before taking Minipress (prazosin)?


You should not use this medication if you are allergic to prazosin or similar medicines such as alfuzosin (Uroxatral), doxazosin (Cardura), silodosin (Rapaflo), tamsulosin (Flomax), or terazosin (Hytrin).

Prazosin can affect your pupils during cataract surgery. Tell your eye surgeon ahead of time that you are using this medication. Do not stop using prazosin before surgery unless your surgeon tells you to.


FDA pregnancy category C. It is not known whether prazosin will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. Prazosin can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

How should I take Minipress (prazosin)?


Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.


Your doctor may occasionally change your dose to make sure you get the best results.


Prazosin lowers blood pressure and may cause dizziness or fainting, especially when you first start taking it or whenever your dose is changed. Call your doctor if you have severe dizziness or feel like you might pass out.

You may feel very dizzy when you first wake up. Be careful when standing or sitting up from a lying position.


Your blood pressure will need to be checked often. Visit your doctor regularly.


Keep using this medicine as directed, even if you feel well. High blood pressure often has no symptoms. You may need to use blood pressure medication for the rest of your life.

Some things can cause your blood pressure to get too low. This includes vomiting, diarrhea, heavy sweating, heart disease, dialysis, a low-salt diet, or taking diuretics (water pills). Tell your doctor if you have a prolonged illness that causes diarrhea or vomiting.


Store at room temperature away from moisture and heat.

See also: Minipress dosage (in more detail)

What happens if I miss a dose?


Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.


What happens if I overdose?


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include extreme drowsiness or fainting.


What should I avoid while taking Minipress (prazosin)?


Prazosin may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.

To prevent dizziness, avoid standing for long periods of time or becoming overheated during exercise and in hot weather.


Avoid getting up too fast from a sitting or lying position, or you may feel dizzy. Get up slowly and steady yourself to prevent a fall.


Drinking alcohol can increase certain side effects of prazosin.

Minipress (prazosin) side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have a serious side effect such as:

  • fast or pounding heartbeats or fluttering in your chest;




  • feeling like you might pass out;




  • trouble breathing;




  • swelling in your hands, ankles, or feet; or




  • penis erection that is painful or lasts 4 hours or longer.



Less serious side effects may include:



  • mild dizziness;




  • weakness, tired feeling, drowsiness;




  • headache; or




  • nausea.



This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect Minipress (prazosin)?


Tell your doctor about all other medications you use, especially:



  • propranolol (Inderal, Innopran); or




  • other blood pressure medications, including diuretics (water pills).



This list is not complete and other drugs may interact with prazosin. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.



More Minipress resources


  • Minipress Side Effects (in more detail)
  • Minipress Dosage
  • Minipress Use in Pregnancy & Breastfeeding
  • Minipress Drug Interactions
  • Minipress Support Group
  • 9 Reviews for Minipress - Add your own review/rating


  • Minipress Prescribing Information (FDA)

  • Minipress MedFacts Consumer Leaflet (Wolters Kluwer)

  • Minipress Monograph (AHFS DI)

  • Minipress Advanced Consumer (Micromedex) - Includes Dosage Information

  • Prazosin Prescribing Information (FDA)

  • Prazosin Professional Patient Advice (Wolters Kluwer)



Compare Minipress with other medications


  • Benign Prostatic Hyperplasia
  • Heart Failure
  • High Blood Pressure
  • Raynaud's Syndrome


Where can I get more information?


  • Your pharmacist can provide more information about prazosin.

See also: Minipress side effects (in more detail)


Neuromuscular blocking agents


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Neuromuscular blocking agents bind to acetylcholine receptors postsynaptically and inhibit the action of acetylcholine. This blocks neuromuscular transmission and causes paralysis of the muscle.


Neuromuscular blocking agents are used as an adjunct to anesthesia, only when artificial ventilation is available, to produce muscle relaxation in order to prevent movement of muscle during surgery.

See also

Medical conditions associated with neuromuscular blocking agents:

  • Anesthesia
  • Light Anesthesia

Drug List:

NNRTIs


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Non-nucleoside reverse transcriptase inhibitors (NNRTI

See also

Medical conditions associated with NNRTIs:

  • HIV Infection
  • Nonoccupational Exposure
  • Occupational Exposure
  • Reduction of Perinatal Transmission of HIV

Drug List:

Clear Away Wart Removal System Topical


Generic Name: salicylic acid (Topical route)


sal-i-SIL-ik AS-id


Commonly used brand name(s)

In the U.S.


  • Akurza

  • Aliclen

  • Avosil

  • Betasal

  • Compound W

  • Corn Removing

  • Dermarest Psoriasis

  • DHS Sal

  • Drytex

  • Duofilm

  • Duoplant

  • Durasal

  • Freezone

  • Fung-O

  • Gets-It Corn/Callus Remover

  • Gordofilm

  • Hydrisalic

  • Ionil

  • Ionil Plus

  • Keralyt

  • Keralyt Scalp

  • Lupicare

  • Mediplast

  • Mg217 Sal-Acid

  • Mosco Corn & Callus Remover

  • Neutrogena

  • Occlusal-HP

  • Off-Ezy

  • Oxy Balance

  • P & S

  • Palmer's Skin Success Acne Cleanser

  • Propa pH

  • Salac

  • Sal-Acid Plaster

  • Salactic Film

  • Salex

  • Salitop

  • Salkera

  • Sal-Plant Gel

  • Salvax

  • Seba-Clear

  • Stri-Dex

  • Thera-Sal

  • Therasoft Anti-Acne

  • Tinamed

  • Ti-Seb

  • Virasal

  • Wart-Off Maximum Strength

  • Zapzyt

In Canada


  • Acnex

  • Acnomel Acne Mask

  • Clear Away Wart Removal System

  • Compound W One-Step Wart Remover

  • Compound W Plus

  • Dr. Scholl's Clear Away One Step Plantar Wart Remover

  • Dr. Scholl's Cushlin Ultra Slim Callus Removers

  • Dr. Scholl's Cushlin Ultra Slim Corn Removers

  • Duoforte 27

  • Freezone - One Step Callus Remover Pad

  • Freezone - One Step Corn Remover Pad

Available Dosage Forms:


  • Soap

  • Lotion

  • Liquid

  • Foam

  • Ointment

  • Gel/Jelly

  • Solution

  • Cream

  • Pad

  • Paste

  • Shampoo

  • Dressing

  • Stick

Therapeutic Class: Antiacne


Pharmacologic Class: NSAID


Chemical Class: Salicylate, Non-Aspirin


Uses For Clear Away Wart Removal System


Salicylic acid is used to treat many skin disorders, such as acne, dandruff, psoriasis, seborrheic dermatitis of the skin and scalp, calluses, corns, common warts, and plantar warts, depending on the dosage form and strength of the preparation.


Some of these preparations are available only with your doctor's prescription.


Before Using Clear Away Wart Removal System


In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Young children may be at increased risk of unwanted effects because of increased absorption of salicylic acid through the skin. Also, young children may be more likely to get skin irritation from salicylic acid. Salicylic acid should not be applied to large areas of the body, used for long periods of time, or used under occlusive dressing (air-tight covering, such as kitchen plastic wrap) in infants and children. Salicylic acid should not be used in children younger than 2 years of age.


Geriatric


Elderly people are more likely to have age-related blood vessel disease. This may increase the chance of problems during treatment with this medicine.


Breast Feeding


There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Using this medicine with any of the following medicines is usually not recommended, but may be required in some cases. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Abciximab

  • Argatroban

  • Bivalirudin

  • Cilostazol

  • Citalopram

  • Clovoxamine

  • Dabigatran Etexilate

  • Dipyridamole

  • Escitalopram

  • Femoxetine

  • Flesinoxan

  • Fluoxetine

  • Fluvoxamine

  • Fondaparinux

  • Heparin

  • Lepirudin

  • Nefazodone

  • Paroxetine

  • Protein C

  • Rivaroxaban

  • Sertraline

  • Sibutramine

  • Ticlopidine

  • Tirofiban

  • Vilazodone

  • Zimeldine

Using this medicine with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Acenocoumarol

  • Anisindione

  • Ardeparin

  • Azilsartan Medoxomil

  • Azosemide

  • Bemetizide

  • Bendroflumethiazide

  • Benzthiazide

  • Bumetanide

  • Buthiazide

  • Candesartan Cilexetil

  • Certoparin

  • Chlorothiazide

  • Chlorthalidone

  • Clopamide

  • Cyclopenthiazide

  • Dalteparin

  • Danaparoid

  • Dicumarol

  • Enoxaparin

  • Eprosartan

  • Ethacrynic Acid

  • Furosemide

  • Hydrochlorothiazide

  • Hydroflumethiazide

  • Indapamide

  • Irbesartan

  • Losartan

  • Methyclothiazide

  • Metolazone

  • Nadroparin

  • Olmesartan Medoxomil

  • Parnaparin

  • Phenindione

  • Phenprocoumon

  • Piretanide

  • Polythiazide

  • Probenecid

  • Reviparin

  • Tamarind

  • Tasosartan

  • Telmisartan

  • Tinzaparin

  • Torsemide

  • Trichlormethiazide

  • Valsartan

  • Warfarin

  • Xipamide

Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.


Other Medical Problems


The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially:


  • Blood vessel disease

  • Diabetes mellitus (sugar diabetes)—Use of this medicine may cause severe redness or ulceration, especially on the hands or feet

  • Inflammation, irritation, or infection of the skin—Use of this medicine may cause severe irritation if applied to inflamed, irritated, or infected area of the skin

  • Influenza (flu) or

  • Varicella (chicken pox)—This medicine should not be used in children and teenagers with the flu or chicken pox. There is a risk of Reye's syndrome.

  • Kidney disease or

  • Liver disease—Using this medicine for a long time over large areas could result in unwanted effects

Proper Use of salicylic acid

This section provides information on the proper use of a number of products that contain salicylic acid. It may not be specific to Clear Away Wart Removal System. Please read with care.


It is very important that you use this medicine only as directed. Do not use more of it, do not use it more often, and do not use it for a longer time than recommended on the label, unless otherwise directed by your doctor. To do so may increase the chance of absorption through the skin and the chance of salicylic acid poisoning.


If your doctor has ordered an occlusive dressing (airtight covering, such as kitchen plastic wrap) to be applied over this medicine, make sure you know how to apply it. Since an occlusive dressing will increase the amount of medicine absorbed through your skin and the possibility of salicylic acid poisoning, use it only as directed. If you have any questions about this, check with your doctor.


Keep this medicine away from the eyes and other mucous membranes, such as the mouth and inside of the nose. If you should accidentally get some in your eyes or on other mucous membranes, immediately flush them with water for 15 minutes.


To use the cream, lotion, or ointment form of salicylic acid:


  • Apply enough medicine to cover the affected area, and rub in gently.

To use the gel form of salicylic acid:


  • Before using salicylic acid gel, apply wet packs to the affected areas for at least 5 minutes. If you have any questions about this, check with your health care professional.

  • Apply enough gel to cover the affected areas, and rub in gently.

To use the pad form of salicylic acid:


  • Wipe the pad over the affected areas.

  • Do not rinse off medicine after treatment.

To use the plaster form of salicylic acid for warts, corns, or calluses:


  • This medicine comes with patient instructions. Read them carefully before using.

  • Do not use this medicine on irritated skin or on any area that is infected or reddened. Also, do not use this medicine if you are a diabetic or if you have poor blood circulation.

  • Do not use this medicine on warts with hair growing from them or on warts on the face, in or on the genital (sex) organs, or inside the nose or mouth. Also do not use on moles or birthmarks. To do so may cause severe irritation.

  • Wash the area to be treated and dry thoroughly. Warts may be soaked in warm water for 5 minutes before drying.

  • Cut the plaster to fit the wart, corn, or callus and apply.

  • For corns and calluses:
    • Repeat every 48 hours as needed for up to 14 days, or as directed by your doctor, until the corn or callus is removed.

    • Corns or calluses may be soaked in warm water for 5 minutes to help in their removal.


  • For warts:
    • Depending on the product, either:
      • Apply plaster and repeat every 48 hours as needed, or
        • Apply plaster at bedtime, leave in place for at least 8 hours, remove plaster in the morning, and repeat every 24 hours as needed.



    • Repeat for up to 12 weeks as needed, or as directed by your doctor, until wart is removed.


  • If discomfort gets worse during treatment or continues after treatment, or if the wart spreads, check with your doctor.

To use the shampoo form of salicylic acid:


  • Before applying this medicine, wet the hair and scalp with lukewarm water. Apply enough medicine to work up a lather and rub well into the scalp for 2 or 3 minutes, then rinse. Apply the medicine again and rinse thoroughly.

To use the soap form of salicylic acid:


  • Work up a lather with the soap, using hot water, and scrub the entire affected area with a washcloth or facial sponge or mitt.

  • If you are to use this soap in a foot bath, work up rich suds in hot water and soak the feet for 10 to 15 minutes. Then pat dry without rinsing.

To use the topical solution form of salicylic acid for acne:


  • Wet a cotton ball or pad with the topical solution and wipe the affected areas.

  • Do not rinse off medicine after treatment.

To use the topical solution form of salicylic acid for warts, corns, or calluses:


  • This medicine comes with patient instructions. Read them carefully before using.

  • This medicine is flammable. Do not use it near heat or open flame or while smoking.

  • Do not use this medicine on irritated skin or on any area that is infected or reddened. Also, do not use this medicine if you are a diabetic or if you have poor blood circulation.

  • Do not use this medicine on warts with hair growing from them or on warts on the face, in or on the genital (sex) organs, or inside the nose or mouth. Also do not use on moles or birthmarks. To do so may cause severe irritation.

  • Avoid breathing in the vapors from the medicine.

  • Wash the area to be treated and dry thoroughly. Warts may be soaked in warm water for 5 minutes before drying.

  • Apply the medicine one drop at a time to completely cover each wart, corn, or callus. Let dry.

  • For warts—Repeat one or two times a day as needed for up to 12 weeks, or as directed by your doctor, until wart is removed.

  • For corns and calluses—Repeat one or two times a day as needed for up to 14 days, or as directed by your doctor, until the corn or callus is removed.

  • Corns and calluses may be soaked in warm water for 5 minutes to help in their removal.

  • If discomfort gets worse during treatment or continues after treatment, or if the wart spreads, check with your doctor.

Unless your hands are being treated, wash them immediately after applying this medicine to remove any medicine that may be on them.


Dosing


The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.


The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.


  • For cream dosage form:
    • For corns and calluses:
      • Adults and children—Use the 2 to 10% cream as needed. Use the 25 to 60% cream one time every three to five days.



  • For gel dosage form:
    • For acne:
      • Adults and children—Use the 0.5 to 5% gel one time a day.


    • For psoriasis:
      • Adults and children—Use the 5% gel one time a day.


    • For common warts:
      • Adults and children—Use the 5 to 26% gel one time a day.



  • For lotion dosage form:
    • For acne:
      • Adults and children—Use the 1 to 2% lotion one to three times a day.


    • For dandruff and antiseborrhic dermatitis of the scalp:
      • Adults and children—Use the 1.8 to 2% lotion on the scalp one or two times a day.



  • For ointment dosage form:
    • For acne:
      • Adults and children—Use the 3 to 6% ointment as needed.


    • For psoriasis and seborrheic dermatitis:
      • Adults and children—Use the 3 to 10% ointment as needed.


    • For common warts:
      • Adults and children—Use the 3 to 10% ointment as needed. Use the 25 to 60% ointment one time every three to five days.



  • For pads dosage form:
    • For acne:
      • Adults and children—Use one to three times a day.



  • For plaster dosage form:
    • For corns, calluses, common warts, or plantar warts:
      • Adults and children—Use one time a day or one time every other day.



  • For shampoo dosage form:
    • For dandruff or seborrheic dermatitis of the scalp:
      • Adults and children—Use on the scalp one or two times a week.



  • For soap dosage form:
    • For acne:
      • Adults and children—Use as needed.



  • For topical solution dosage form:
    • For acne:
      • Adults and children—Use the 0.5 to 2% topical solution one to three times a day.


    • For common warts and plantar warts:
      • Adults and children—Use the 5 to 27% topical solution one or two times a day.


    • For corns and calluses:
      • Adults and children—Use the 12 to 27% topical solution one or two times a day.



Missed Dose


If you miss a dose of this medicine, apply it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule.


Storage


Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Precautions While Using Clear Away Wart Removal System


When using salicylic acid, do not use any of the following preparations on the same affected area as this medicine, unless otherwise directed by your doctor:


  • Abrasive soaps or cleansers

  • Alcohol-containing preparations

  • Any other topical acne preparation or preparation containing a peeling agent (for example, benzoyl peroxide, resorcinol, sulfur, or tretinoin [vitamin A acid])

  • Cosmetics or soaps that dry the skin

  • Medicated cosmetics

  • Other topical medicine for the skin

To use any of the above preparations on the same affected area as salicylic acid may cause severe irritation of the skin.


Check with your doctor right away if you have nausea, vomiting, dizziness, loss of hearing, tinnitus, lethargy hyperpnea, diarrhea, and psychic disturbances. These could be symptoms of a serious condition called salicylate toxicity, especially in children under 12 years of age and patients with kidney or liver problems.


Clear Away Wart Removal System Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Check with your doctor as soon as possible if any of the following side effects occur:


Less common or rare
  • Skin irritation not present before use of this medicine (moderate or severe)

Frequency not known
  • Dryness and peeling of skin

  • flushing

  • redness of skin

  • unusually warm skin

Symptoms of salicylic acid poisoning
  • Confusion

  • diarrhea

  • dizziness

  • fast or deep breathing

  • headache (severe or continuing)

  • hearing loss

  • lightheadedness

  • nausea

  • rapid breathing

  • ringing or buzzing in ears (continuing)

  • severe drowsiness

  • stomach pain

  • vomiting

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


More common
  • Skin irritation not present before use of this medicine (mild)

  • stinging

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.



The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.


The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.


More Clear Away Wart Removal System Topical resources


  • Clear Away Wart Removal System Topical Use in Pregnancy & Breastfeeding
  • Clear Away Wart Removal System Topical Drug Interactions
  • 0 Reviews for Clear Away Wart Removal Topical - Add your own review/rating


Compare Clear Away Wart Removal System Topical with other medications


  • Acne
  • Dermatological Disorders
  • Warts

Natural penicillins


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Natural Penicillins were the first antibiotics used in clinical practice. They are based on the original penicillin- G structure. They inhibit bacterial cell wall synthesis and are generally bactericidal.


Natural penicillins are effective against gram positive bacteria such as staphylococci, streptococci and gram negative bacteria such as meningococci, Treponema, Borrelia and Leptospira.

See also

Medical conditions associated with natural penicillins:

  • Actinomycosis
  • Anthrax
  • Anthrax Prophylaxis
  • Aspiration Pneumonia
  • Bacterial Infection
  • Clostridial Infection
  • Congenital Syphilis
  • Cutaneous Bacillus anthracis
  • Deep Neck Infection
  • Diphtheria
  • Endocarditis
  • Fusospirochetosis, Trench Mouth
  • Joint Infection
  • Leptospirosis
  • Lyme Disease, Arthritis
  • Lyme Disease, Carditis
  • Lyme Disease, Erythema Chronicum Migrans
  • Lyme Disease, Neurologic
  • Meningitis
  • Meningitis, Meningococcal
  • Meningitis, Pneumococcal
  • Neurosyphilis
  • Otitis Media
  • Pneumonia
  • Prevention of Perinatal Group B Streptococcal Disease
  • Rat-bite Fever
  • Rheumatic Fever Prophylaxis
  • Skin Infection
  • Strep Throat
  • Streptococcal Infection
  • Syphilis, Early
  • Syphilis, Latent
  • Tertiary Syphilis
  • Tonsillitis/Pharyngitis
  • Upper Respiratory Tract Infection

Drug List:

Misostol




Misostol may be available in the countries listed below.


Ingredient matches for Misostol



Mitoxantrone

Mitoxantrone is reported as an ingredient of Misostol in the following countries:


  • Brazil

  • Venezuela

Mitoxantrone dihydrochloride (a derivative of Mitoxantrone) is reported as an ingredient of Misostol in the following countries:


  • Chile

International Drug Name Search

Anacort




Anacort may be available in the countries listed below.


Ingredient matches for Anacort



Hydrocortisone

Hydrocortisone 21-(hydrogen succinate) (a derivative of Hydrocortisone) is reported as an ingredient of Anacort in the following countries:


  • Bangladesh

International Drug Name Search

Neuronal potassium channel openers


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

See also

Medical conditions associated with neuronal potassium channel openers:

  • Epilepsy
  • Seizures

Drug List:

Obagi Skin Lightening Complex





Dosage Form: lotion
Obagi® Skin Lightening Complex

(Hydroquinone USP, 4%)

Skin Bleaching Cream

Rx Only

FOR EXTERNAL USE ONLY



INGREDIENTS


Each gram of Skin Lightening Complex contains Hydroquinone USP 40 mg/g in a base of Ascorbic Acid, BHT, Cetyl Alcohol, Disodium EDTA, Glycerin, Lactic Acid, Methylparaben, Phenyl Trimethicone, PPG-2 Myristyl Ether Propionate, Propylparaben, Saponins, Sodium Lauryl Sulfate, Sodium Metabisulfite, TEA-Salicylate, Tocopheryl Acetate and Water.



Obagi Skin Lightening Complex Description


Hydroquinone is 1,4-benzenediol. The drug is freely soluble in water and in alcohol. Chemically, hydroquinone is designated as p-dihydroxybenzene; the empirical formula is C6H6O2; the molecular weight is 110.11 g/mol. The chemical structure is the diagram to the right.




Obagi Skin Lightening Complex - Clinical Pharmacology


Topical application of hydroquinone produces a reversible depigmentation of the skin by inhibition of the enzymatic oxidation of tyrosine to 3, 4-dihydroxyphenylalanine (dopa) and suppression of other melanocyte metabolic processes.


Exposure to sunlight or ultraviolet light will cause repigmentation of the bleached areas, which may be prevented by the use of sunblocking agents or sunscreen agents.



Indications and Usage for Obagi Skin Lightening Complex


For the gradual bleaching of hyperpigmented skin conditions such as chloasma, melasma, freckles, senile lentigines, and other unwanted areas of melanin hyperpigmentation.



Contraindications


People with prior history of sensitivity or allergic reaction to this product or any of its ingredients should not use it. The safety of topical hydroquinone use during pregnancy or in children (12 years and under) has not been established.



Obagi Skin Lightening Complex Dosage and Administration


A thin application should be applied to the chest and neck area twice daily or as directed by a physician. If no improvement is seen after 8-12 weeks of treatment, use of this product should be discontinued. Sun exposure should be limited by using a sunscreen agent, a sunblocking agent, or protective clothing to cover bleached skin when using and after using this product in order to prevent repigmentation.



Warnings


Hydroquinone is a skin bleaching agent, which may produce unwanted cosmetic effects if not used as directed. The physician should be familiar with the contents of this insert before prescribing or dispensing this medication.


Test for skin sensitivity before using by applying a small amount to an unbroken patch of skin and check within 24 hours. Minor redness is not a contraindication, but where there is itching or vesicle formation or excessive inflammatory response, the product should be discontinued and a physician consulted. Close patient supervision is recommended.


Avoid contact with the eyes, nose, mouth, or lips. In case of accidental contact, the patient should rinse the eyes, nose, mouth, or lips with water and contact a physician.


Sunscreen use is an essential aspect of hydroquinone therapy because even minimal sunlight exposure sustains melanocytic activity.


Contains sodium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. The overall prevalence of sulfite sensitivity in the general population is unknown and probably low. Sulfite sensitivity is seen more frequently in asthmatic than in nonasthmatic people.



Precautions


(ALSO SEE WARNINGS)


Treatment should be limited to relatively small areas of the body at one time since some patients experience a transient skin reddening and a mild burning sensation, which does not preclude treatment.



PREGNANCY CATEGORY C


Animal reproduction studies have not been conducted with topical hydroquinone. It is also not known whether hydroquinone can cause fetal harm when used topically on a pregnant woman or affect reproductive capacity. It is not known to what degree, if any, topical hydroquinone is absorbed systemically. Topical hydroquinone should be used on pregnant women only when clearly indicated.



NURSING MOTHERS


It is not known whether topical hydroquinone is absorbed or excreted in human milk. Caution is advised when topical hydroquinone is used by a nursing mother.



PEDIATRIC USAGE


Safety and effectiveness in children below the age of 12 years have not been established.



Adverse Reactions


No systemic adverse reactions have been reported. Occasional hypersensitivity (localized contact dermatitis) may occur, in which case the product should be discontinued and the physician notified immediately.



How is Obagi Skin Lightening Complex Supplied


Obagi Skin Lightening Complex is available as follows:


2.0 oz (57 g) tube

NDC 63032-120-60



Store at controlled room temperature:

15°-25°C (59°F-77°F)



OBAGI®

MEDICAL


Obagi is a registered trademark of OMP, Inc.

Distributed by OMP, Inc.

Obagi Medical Products, Inc.

Long Beach, CA 90806

USA

www.obagi.com

60650611X



PRINCIPAL DISPLAY PANEL - 57 g Carton


NDC 62032-120-60


OBAGI®

MEDICAL


ELASTIderm®

décolletage


Chest and Neck


Skin

Lightening

Complex


Hydroquinone USP, 4%

Rx Only


NET WT 2.0 OZ. (57 g)










ELASTIDERM DECOLLETAGE SKIN LIGHTENING COMPLEX   CHEST AND NECK
hydroquinone  lotion










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)62032-120
Route of AdministrationTOPICALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (HYDROQUINONE)HYDROQUINONE40 mg  in 1 g
































Inactive Ingredients
Ingredient NameStrength
EDETATE DISODIUM 
TROLAMINE SALICYLATE 
SODIUM LAURYL SULFATE 
CETYL ALCOHOL 
GLYCERIN 
LACTIC ACID 
ALPHA-TOCOPHEROL ACETATE 
ASCORBIC ACID 
SODIUM METABISULFITE 
WATER 
METHYLPARABEN 
PROPYLPARABEN 
BUTYLATED HYDROXYTOLUENE 
PHENYL TRIMETHICONE 


















Product Characteristics
ColorGRAYScore    
ShapeSize
FlavorImprint Code
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
162032-120-601 TUBE In 1 CARTONcontains a TUBE
157 g In 1 TUBEThis package is contained within the CARTON (62032-120-60)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
UNAPPROVED DRUG OTHER12/01/2010


Labeler - OMP, INC. (790553353)









Establishment
NameAddressID/FEIOperations
PURETEK CORPORATION785961046MANUFACTURE, LABEL, PACK
Revised: 12/2011OMP, INC.