Maxima

Maxima may be available in the countries listed below.

Ingredient matches for Maxima

Esomeprazole

Esomeprazole is reported as an ingredient of Maxima in the following countries:

• Bangladesh

International Drug Name Search

Sertindole

Scheme

Rec.INN

ATC (Anatomical Therapeutic Chemical Classification)

N05AE03

CAS registry number (Chemical Abstracts Service)

0106516-24-9

Chemical Formula

C24-H26-Cl-F-N4-O

Molecular Weight

440

Therapeutic Category

Neuroleptic

Chemical Name

2-Imidazolidinone, 1-[2-[4-[5-chloro-1-(4-fluorophenyl)-1H-indol-3-yl]-1-piperidinyl]ethyl]-

Foreign Names

• Sertindolum (Latin)
• Sertindol (German)
• Sertindole (French)
• Sertindol (Spanish)

Generic Names

• Sertindole (OS: BAN, USAN)
• Lu 23-174 (IS: Lundbeck)

Brand Names

• Serdolect
  Lundbeck, Austria; Lundbeck, Belgium; Lundbeck, Bulgaria; Lundbeck, Switzerland; Lundbeck, Czech Republic; Lundbeck, Germany; Lundbeck, Denmark; Lundbeck, Estonia; Lundbeck, Spain; Lundbeck, Finland; Lundbeck, Croatia (Hrvatska); Lundbeck, Hungary; Lundbeck, Ireland; Lundbeck, Lithuania; Lundbeck, Luxembourg; Lundbeck, Latvia; Lundbeck, Netherlands; Lundbeck, Norway; Lundbeck, Oman; Lundbeck, Poland; Lundbeck, Russian Federation; Lundbeck, Sweden; Lundbeck, Slovakia; Lundbeck, Turkey

International Drug Name Search

Glossary

BAN	British Approved Name
IS	Inofficial Synonym
OS	Official Synonym
Rec.INN	Recommended International Nonproprietary Name (World Health Organization)
USAN	United States Adopted Name

Click for further information on drug naming conventions and International Nonproprietary Names.

Brintenal

Brintenal may be available in the countries listed below.

Ingredient matches for Brintenal

Selegiline

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

• Argentina

International Drug Name Search

Limclair

Limclair may be available in the countries listed below.

Ingredient matches for Limclair

Edetic Acid

Edetic Acid trisodium salt (a derivative of Edetic Acid) is reported as an ingredient of Limclair in the following countries:

• Ireland

International Drug Name Search

Mebidrolina

Mebidrolina may be available in the countries listed below.

Ingredient matches for Mebidrolina

Mebhydrolin

Mebidrolina (DCIT) is also known as Mebhydrolin (Rec.INN)

International Drug Name Search

Glossary

DCIT	Denominazione Comune Italiana
Rec.INN	Recommended International Nonproprietary Name (World Health Organization)

Click for further information on drug naming conventions and International Nonproprietary Names.

Gévatran

Gévatran may be available in the countries listed below.

Ingredient matches for Gévatran

Naftidrofuryl

Naftidrofuryl oxalate (a derivative of Naftidrofuryl) is reported as an ingredient of Gévatran in the following countries:

• France

International Drug Name Search

Zomcare

Zomcare may be available in the countries listed below.

Ingredient matches for Zomcare

Omeprazole

Omeprazole is reported as an ingredient of Zomcare in the following countries:

• India

International Drug Name Search

Vagi-Hex

Vagi-Hex may be available in the countries listed below.

Ingredient matches for Vagi-Hex

Hexetidine

Hexetidine is reported as an ingredient of Vagi-Hex in the following countries:

• Germany


• Switzerland


• Turkey

International Drug Name Search

Oyster Shell Calcium

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 (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 (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 (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 (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 (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 (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 (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 resources

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

• Calcium Carbonate MedFacts Consumer Leaflet (Wolters Kluwer)


• Titralac Consumer Overview


• Titralac MedFacts Consumer Leaflet (Wolters Kluwer)


• Tums Chewable Tablets MedFacts Consumer Leaflet (Wolters Kluwer)

Compare Oyster Shell Calcium with other medications

• Dietary Supplementation
• Osteoporosis

Where can I get more information?

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

Hivisco

Hivisco may be available in the countries listed below.

Ingredient matches for Hivisco

Hyaluronic Acid

Hyaluronic Acid sodium salt (a derivative of Hyaluronic Acid) is reported as an ingredient of Hivisco in the following countries:

• Japan

International Drug Name Search

Hapstar ID

Hapstar ID may be available in the countries listed below.

Ingredient matches for Hapstar ID

Indometacin

Indometacin is reported as an ingredient of Hapstar ID in the following countries:

• Japan

International Drug Name Search

Spalox

Spalox may be available in the countries listed below.

Ingredient matches for Spalox

Scopolamine

Scopolamine butylbromide (a derivative of Scopolamine) is reported as an ingredient of Spalox in the following countries:

• Thailand

Sparfloxacin

Sparfloxacin is reported as an ingredient of Spalox in the following countries:

• Bangladesh

International Drug Name Search

Orphenadrine w/A.C.

Generic Name: orphenadrine, aspirin, and caffeine (Oral route)

or-FEN-a-dreen SIT-rate, AS-pir-in, KAF-een

Commonly used brand name(s)

In the U.S.

• Norgesic


• Norgesic Forte


• Orphenadrine w/A.C.


• Orphengesic


• Orphengesic Forte

Available Dosage Forms:

• Tablet

Therapeutic Class: Skeletal Muscle Relaxant, Centrally Acting/Salicylate, Aspirin Combination

Pharmacologic Class: Orphenadrine

Chemical Class: Salicylate, Aspirin

Uses For Orphenadrine w/A.C.

Orphenadrine and aspirin combination is used to help relax certain muscles in your body and relieve the pain and discomfort caused by strains, sprains, or other injury to your muscles. However, this medicine does not take the place of rest, exercise, or other treatment that your doctor may recommend for your medical problem.

Orphenadrine acts in the central nervous system (CNS) to produce its muscle relaxant effects. Actions in the CNS may also be responsible for some of its side effects. Orphenadrine also has other actions (antimuscarinic) that may be responsible for some of its side effects.

This combination medicine also contains caffeine.

In the U.S., this combination medicine is available only with your doctor's prescription.

Before Using Orphenadrine w/A.C.

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

Do not give a medicine containing aspirin to a child or a teenager with a fever or other symptoms of a virus infection, especially flu or chickenpox, without first discussing its use with your child's doctor. This is very important because aspirin may cause a serious illness called Reye's syndrome in children with fever caused by a virus infection, especially flu or chickenpox. Children who do not have a virus infection may also be more sensitive to the effects of aspirin, especially if they have a fever or have lost large amounts of body fluid because of vomiting, diarrhea, or sweating. This may increase the chance of side effects during treatment.

There is no specific information about the use of orphenadrine in children.

Geriatric

Elderly people are especially sensitive to the effects of aspirin. This may increase the chance of side effects during treatment.

There is no specific information about the use of orphenadrine in the elderly.

Pregnancy

	Pregnancy Category	Explanation
All Trimesters	D	Studies in pregnant women have demonstrated a risk to the fetus. However, the benefits of therapy in a life threatening situation or a serious disease, may outweigh the potential risk.

Breast Feeding

AspirinOrphenadrine

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.

Caffeine

Studies in women suggest that this medication poses minimal risk to the infant when used during 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 not recommended. Your doctor may decide not to treat you with this medication or change some of the other medicines you take.

• Influenza Virus Vaccine, Live


• Ketorolac

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.

• Acenocoumarol


• Alteplase, Recombinant


• Anisindione


• Beta Glucan


• Cilostazol


• Citalopram


• Clovoxamine


• Dabigatran Etexilate


• Desirudin


• Desvenlafaxine


• Dicumarol


• Duloxetine


• Eptifibatide


• Escitalopram


• Femoxetine


• Flesinoxan


• Fluoxetine


• Fluvoxamine


• Ginkgo


• Heparin


• Ketoprofen


• Methotrexate


• Milnacipran


• Naproxen


• Nefazodone


• Paroxetine


• Phenindione


• Phenprocoumon


• Reteplase, Recombinant


• Rivaroxaban


• Sertraline


• Ticlopidine


• Varicella Virus Vaccine


• Venlafaxine


• Vilazodone


• Warfarin


• 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.

• Anagrelide


• Ardeparin


• Azosemide


• Bemetizide


• Bendroflumethiazide


• Benzthiazide


• Betamethasone


• Bumetanide


• Buthiazide


• Captopril


• Celecoxib


• Certoparin


• Chlorothiazide


• Chlorpropamide


• Chlorthalidone


• Clopamide


• Cortisone


• Cyclopenthiazide


• Dalteparin


• Danaparoid


• Deflazacort


• Delapril


• Dexamethasone


• Diltiazem


• Enalaprilat


• Enalapril Maleate


• Enoxaparin


• Ethacrynic Acid


• Furosemide


• Glyburide


• Hydrochlorothiazide


• Hydroflumethiazide


• Ibuprofen


• Imidapril


• Indapamide


• Lisinopril


• Methyclothiazide


• Methylprednisolone


• Metolazone


• Nadroparin


• Nitroglycerin


• Paramethasone


• Parnaparin


• Perphenazine


• Piretanide


• Polythiazide


• Prednisolone


• Prednisone


• Probenecid


• Reviparin


• Rofecoxib


• Streptokinase


• Tamarind


• Temocapril


• Tenecteplase


• Tinzaparin


• Tirofiban


• Tolbutamide


• Torsemide


• Triamcinolone


• Trichlormethiazide


• Valproic Acid


• Verapamil


• 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. 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 may cause an increased risk of certain side effects but may be unavoidable in some cases. If used together, your doctor may change the dose or how often you use this medicine, or give you special instructions about the use of food, alcohol, or tobacco.

• Ethanol

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:

• Anemia or


• Overactive thyroid or


• Stomach ulcer or other stomach problems—Aspirin may make your condition worse

• Asthma, allergies, and nasal polyps, history of or


• Glucose-6-phosphate dehydrogenase (G6PD) deficiency or


• Kidney disease or


• Liver disease—The chance of side effects may be increased

• Disease of the digestive tract, especially esophagus disease or intestinal blockage, or


• Enlarged prostate or


• Fast or irregular heartbeat or


• Glaucoma or


• Myasthenia gravis or


• Urinary tract blockage—Orphenadrine has side effects that may be harmful to people with these conditions

• Gout—Aspirin can make this condition worse and can also lessen the effects of some medicines used to treat gout

• Heart disease—The chance of some side effects may be increased. Also, the caffeine present in this combination medicine can make your condition worse

• Hemophilia or other bleeding problems or


• Vitamin K deficiency—Aspirin may increase the chance of bleeding

Proper Use of orphenadrine, aspirin, and caffeine

This section provides information on the proper use of a number of products that contain orphenadrine, aspirin, and caffeine. It may not be specific to Orphenadrine w/A.C.. Please read with care.

Take this medicine with food or a full glass (8 ounces) of water to lessen stomach irritation.

Do not take this medicine if it has a strong vinegar-like odor. This odor means the aspirin in it is breaking down. If you have any questions about this, check with your health care professional.

Do not take more of this medicine than your doctor ordered to lessen the chance of side effects or overdose.

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 oral dosage forms (tablets):
  
  • For muscle pain and stiffness:
    
    • Adults and teenagers—One or two tablets containing 25 milligrams (mg) of orphenadrine and 385 mg of aspirin, or one-half or one tablet containing 50 mg of orphenadrine and 770 mg of aspirin, three or four times a day.
    
    
    • Children—Dose must be determined by your doctor.
    
    
  
  

Missed Dose

If you miss a dose of this medicine, take 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. Do not double doses.

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 Orphenadrine w/A.C.

If you will be taking this medicine for a long time (for example, more than a few weeks), your doctor should check your progress at regular visits.

Check the labels of all nonprescription (over-the-counter [OTC]) and prescription medicines you now take. If any contain orphenadrine or aspirin or other salicylates be especially careful, since taking them while taking this medicine may lead to overdose. If you have any questions about this, check with your health care professional.

Too much use of acetaminophen or certain other medicines together with the aspirin in this combination medicine may increase the chance of unwanted effects. The risk depends on how much of each medicine you take every day, and on how long you take the medicines together. If your doctor directs you to take these medicines together on a regular basis, follow his or her directions carefully. However, do not take acetaminophen or any of the following medicines together with this combination medicine for more than a few days, unless your doctor has directed you to do so and is following your progress:

• Diclofenac (e.g., Voltaren)


• Diflunisal (e.g., Dolobid)


• Etodolac (e.g., Lodine)


• Fenoprofen (e.g., Nalfon)


• Floctafenine (e.g., Idarac)


• Flurbiprofen, oral (e.g., Ansaid)


• Ibuprofen (e.g., Motrin)


• Indomethacin (e.g., Indocin)


• Ketoprofen (e.g., Orudis)


• Ketorolac (e.g., Toradol)


• Meclofenamate (e.g., Meclomen)


• Mefenamic acid (e.g., Ponstel)


• Nabumetone (e.g., Relafen)


• Naproxen (e.g., Naprosyn)


• Oxaprozin (e.g., Daypro)


• Phenylbutazone (e.g., Butazolidin)


• Piroxicam (e.g., Feldene)


• Sulindac (e.g., Clinoril)


• Tenoxicam (e.g., Mobiflex)


• Tiaprofenic acid (e.g., Surgam)


• Tolmetin (e.g., Tolectin)

For diabetic patients:

• The aspirin in this combination medicine may cause false urine sugar test results if you are regularly taking 6 or more of the regular-strength tablets or 3 or more of the double-strength tablets of this medicine a day. Smaller doses or occasional use of aspirin usually will not affect urine sugar tests. If you have any questions about this, check with your health care professional especially if your diabetes is not well controlled.

Do not take this medicine for 5 days before any surgery, including dental surgery, unless otherwise directed by your medical doctor or dentist. Taking aspirin during this time may cause bleeding problems.

The orphenadrine in this combination medicine may add to the effects of alcohol and other CNS depressants (medicines that slow down the nervous system, possibly causing drowsiness). Some examples of CNS depressants are antihistamines or medicine for hay fever, other allergies, or colds; sedatives, tranquilizers, or sleeping medicine; prescription pain medicine or narcotics; barbiturates; medicine for seizures; other muscle relaxants; or anesthetics, including some dental anesthetics. Also, stomach problems may be more likely to occur if you drink alcoholic beverages while you are taking aspirin. Do not drink alcoholic beverages, and check with your doctor before taking any of the medicines listed above, while you are using this medicine.

This medicine may cause some people to have blurred vision or to become drowsy, dizzy, lightheaded, faint, or less alert than they are normally. Make sure you know how you react to this medicine before you drive, use machines, or do anything else that could be dangerous if you are dizzy or are not alert.

Dryness of the mouth may occur while you are taking this medicine. For temporary relief, use sugarless candy or gum, melt bits of ice in your mouth, or use a saliva substitute. However, if dry mouth continues for more than 2 weeks, check with your dentist. Continuing dryness of the mouth may increase the chance of dental disease, including tooth decay, gum disease, and fungus infections.

If you think that you or someone else may have taken an overdose of this medicine, get emergency help at once. Taking an overdose of this medicine may cause unconsciousness or death. Signs of overdose include convulsions (seizures), hearing loss, confusion, ringing or buzzing in the ears, severe drowsiness or tiredness, severe excitement or nervousness, and fast or deep breathing.

Orphenadrine w/A.C. 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.

Get emergency help immediately if any of the following symptoms of overdose occur:

Symptoms of overdose in children

• Changes in behavior


• drowsiness or tiredness (severe)


• fast or deep breathing

• Any loss of hearing


• bloody urine


• confusion


• convulsions (seizures)


• diarrhea


• dizziness or lightheadedness (severe)


• drowsiness (severe)


• excitement or nervousness (severe)


• fast or deep breathing


• hallucinations (seeing, hearing, or feeling things that are not there)


• headache (severe or continuing)


• increased sweating


• nausea or vomiting (severe or continuing)


• ringing or buzzing in the ears (continuing)


• uncontrollable flapping movements of the hands, especially in elderly patients


• unexplained fever


• unusual thirst


• vision problems

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

Less common or rare

• Abdominal or stomach pain, cramping, or burning (severe)


• bloody or black, tarry stools


• decreased urination


• eye pain


• fainting


• fast or pounding heartbeat


• shortness of breath, troubled breathing, tightness in chest, or wheezing


• skin rash, hives, itching, or redness


• sores, ulcers, or white spots on lips or in mouth


• swollen and/or painful glands


• unusual bleeding or bruising


• unusual tiredness or weakness


• vomiting of blood or material that looks like coffee grounds

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

• Abdominal or stomach cramps, pain, or discomfort (mild to moderate)


• dryness of mouth


• heartburn or indigestion


• nausea or vomiting (mild)

Less common

• Blurred or double vision or other vision problems


• confusion


• constipation


• difficult urination


• dizziness or lightheadedness


• drowsiness


• excitement, nervousness, or restlessness


• headache


• muscle weakness


• trembling


• unusually large pupils of eyes

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 Orphenadrine w/A.C. resources

• Orphenadrine w/A.C. Use in Pregnancy & Breastfeeding
• Drug Images
• Orphenadrine w/A.C. Drug Interactions
• Orphenadrine w/A.C. Support Group
• 6 Reviews for Orphenadrine w/A.C. - Add your own review/rating

Compare Orphenadrine w/A.C. with other medications

• Muscle Pain
• Muscle Spasm

Regranex

In the US, Regranex (becaplermin topical) is a member of the drug class miscellaneous topical agents.

US matches:

• Regranex


• Regranex Topical

UK matches:

• Regranex 0.01% gel (SPC)

Ingredient matches for Regranex

Becaplermin

Becaplermin is reported as an ingredient of Regranex in the following countries:

• Austria


• Canada


• France


• Germany


• Israel


• Mexico


• Netherlands


• Slovakia


• Spain


• Switzerland


• Taiwan


• United Kingdom

International Drug Name Search

Glossary

SPC	Summary of Product Characteristics (UK)

Click for further information on drug naming conventions and International Nonproprietary Names.

Oxygen Helium Mixture

Dosage Form: gas
Helium Oxygen Mix Label

COMPRESSED GAS , OXIDIZING, N.O.S. (70% HELIUM USP, 30% OXYGEN USP) UN 3156

NON-FLAMMABLE GAS  2    OXIDIZER 5.1

34313 (01/09)     OXYGEN CONTENT OVER 23.5%

Rx only. CAUTION: Federal law prohibits dispensing without prescription. WARNING: Administration of this gas may be hazardous or contraindicated. For use only by or under supervision of a licensed practitioner who is experienced in the use and administration of gas mixtures, and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindications, and side effects and the precautions to be taken. WARNING: HIGH PRESSURE OXIDIZING GAS. MAY VIGOROUSLY ACCELERATE COMBUSTION. Store and use with adequate ventilation. Keep oil and grease away. Use only with equipment cleaned for oxygen service and rated for cylinder pressure. Use a back flow preventive device in the piping. Cylinder temperatures should not exceed 52C (125F). Open valve slowly. Close valve after each use and when empty. Use in accordance with the Material Safety Data Sheet (MSDS). FIRST AID: IF INHALED, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Call a physician.  HELIUM CAS: 7440-59-7   OXYGEN CAS: 7782-44-7

DO NOT REMOVE THIS PRODUCT LABEL.

Cylinders must be refilled by:

Encompass Medical and Specialty Gases, LTD. 4646 Linden Road P.O. Box 5404 Rockford, IL 61109

CONTENTS:  LTRS    CU. FT.

HELIUM OXYGEN MIX  helium oxygen mix  gas

Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 48883-007 Route of Administration RESPIRATORY (INHALATION) DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Helium (Helium) Helium 500 mL  in 1 L Oxygen (Oxygen) Oxygen 500 mL  in 1 L

Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 48883-007-01 617 L In 1 CYLINDER None 2 48883-007-02 623 L In 1 CYLINDER None 3 48883-007-03 629 L In 1 CYLINDER None 4 48883-007-04 640 L In 1 CYLINDER None 5 48883-007-05 654 L In 1 CYLINDER None 6 48883-007-06 5689 L In 1 CYLINDER None 7 48883-007-07 5743 L In 1 CYLINDER None 8 48883-007-08 5796 L In 1 CYLINDER None 9 48883-007-09 5904 L In 1 CYLINDER None 10 48883-007-10 6009 L In 1 CYLINDER None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved medical gas		04/15/2009

Labeler - Encompass Medical & Specialty Gases Ltd (963344143)

Establishment
Name	Address	ID/FEI	Operations
Encompass Medical & Specialty Gases Ltd		963344143	manufacture

Establishment
Name	Address	ID/FEI	Operations
Encompass Medical & Specialty Gases Ltd		963719286	manufacture

Establishment
Name	Address	ID/FEI	Operations
Encompass Medical & Specialty Gases Ltd		963719096	manufacture

Establishment
Name	Address	ID/FEI	Operations
Encompass Medical & Specialty Gases Ltd		963718361	manufacture

Revised: 12/2011Encompass Medical & Specialty Gases Ltd

Robinul Forte

Pronunciation: GLYE-koe-PIR-oh-late
Generic Name: Glycopyrrolate
Brand Name: Robinul and Robinul Forte

Robinul Forte is used for:

Treating peptic ulcers in combination with other medicines. It may also be used for other conditions as determined by your doctor.

Robinul Forte is an anticholinergic. It works by blocking the activity of a certain substance (acetylcholine) in the body, which decreases stomach acid secretion.

Do NOT use Robinul Forte if:

• you are allergic to any ingredient in Robinul Forte


• you have glaucoma, urinary blockage (eg, inability to urinate), certain stomach or bowel problems (eg, stomach or bowel blockage, bowel paralysis, severe ulcerative colitis, toxic megacolon), myasthenia gravis, or heart problems caused by bleeding


• you are taking a solid oral doseform of potassium (eg, a tablet)

Contact your doctor or health care provider right away if any of these apply to you.

Before using Robinul Forte:

Some medical conditions may interact with Robinul Forte. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding


• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement


• if you have allergies to medicines, foods, or other substances


• if you have nerve problems (eg, autonomic neuropathy), prostate problems, trouble urinating, liver problems, kidney problems, increased pressure in the eyes, an overactive thyroid, or a family history of glaucoma


• if you have heart problems (eg, coronary heart disease, heart failure), a fast or irregular heartbeat, or high blood pressure


• if you have stomach or bowel problems (eg, ulcerative colitis), hiatal hernia along with reflux disease, constipation or diarrhea, or if you have an ileostomy or colostomy


• if you are in poor health

Some MEDICINES MAY INTERACT with Robinul Forte. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Solid oral potassium products (eg, tablets) because the risk of stomach or bowel irritation may be increased by Robinul Forte


• Anticholinergics (eg, benztropine), phenothiazines (eg, chlorpromazine), or tricyclic antidepressants (eg, amitriptyline) because they may increase the risk of Robinul Forte's side effects

This may not be a complete list of all interactions that may occur. Ask your health care provider if Robinul Forte may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Robinul Forte:

Use Robinul Forte as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Take Robinul Forte by mouth with or without food.


• If you miss a dose of Robinul Forte, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Robinul Forte.

Important safety information:

• Robinul Forte may cause drowsiness, dizziness, or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Robinul Forte with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


• Check with your doctor before you drink alcohol or use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are using Robinul Forte; it may add to their effects. Ask your pharmacist if you have questions about which medicines may cause drowsiness.


• Drinking fluids, maintaining good oral hygiene, and sucking on hard sugarless candy can help relieve dry mouth.


• Do not become overheated in hot weather or while you are being active; heatstroke may occur.


• Use Robinul Forte with extreme caution if you have a fever because heatstroke caused by decreased sweating may occur.


• Robinul Forte may make your eyes more sensitive to sunlight. It may help to wear sunglasses.


• Use Robinul Forte with caution in the ELDERLY; they may be more sensitive to its effects.


• Caution is advised when using Robinul Forte in CHILDREN; they may be more sensitive to its effects.


• Robinul Forte should not be used in CHILDREN younger than 12 years old; safety and effectiveness in these children have not been confirmed.


• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Robinul Forte while you are pregnant. It is not known if Robinul Forte is found in breast milk. Robinul Forte may decrease milk production. If you are or will be breast-feeding while you use Robinul Forte, check with your doctor. Discuss any possible risks to your baby, as well as any questions or concerns about this information.

Possible side effects of Robinul Forte:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Bloated feeling; blurred vision; constipation; decreased sweating; dizziness; drowsiness; dry mouth; dry skin; enlarged pupils; headache; loss of taste; nausea; nervousness; sleeplessness; weakness.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); chest pain; confusion; decreased sexual ability; diarrhea; difficulty focusing the eyes; difficulty urinating; excitement; fainting; fast, slow, or irregular heartbeat; seizures; severe or persistent dizziness, light-headedness, or headache; shortness of breath; unusual weakness; vomiting.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Robinul Forte side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include blurred vision; confusion; difficulty breathing; enlarged pupils; excessive thirst; flushed, hot, dry skin; muscle weakness; nausea; paralysis; restlessness; seizures; severe dry mouth; unusual dizziness or drowsiness; vomiting.

Proper storage of Robinul Forte:

Store Robinul Forte at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Robinul Forte out of the reach of children and away from pets.

General information:

• If you have any questions about Robinul Forte, please talk with your doctor, pharmacist, or other health care provider.


• Robinul Forte is to be used only by the patient for whom it is prescribed. Do not share it with other people.


• If your symptoms do not improve or if they become worse, check with your doctor.


• Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Robinul Forte. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Robinul Forte resources

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

• Robinul Forte Advanced Consumer (Micromedex) - Includes Dosage Information


• Glycopyrrolate Professional Patient Advice (Wolters Kluwer)


• Glycopyrrolate Monograph (AHFS DI)


• Cuvposa Consumer Overview


• Cuvposa Prescribing Information (FDA)


• Robinul Prescribing Information (FDA)

Compare Robinul Forte with other medications

• Anesthesia
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Trilam

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OxyContin Sustained-Release Tablets

Pronunciation: OX-i-KOE-done
Generic Name: Oxycodone
Brand Name: OxyContin

OxyContin Sustained-Release Tablets are a narcotic pain reliever that is similar to morphine and is used for around-the-clock treatment of moderate or severe pain. It should not be used to treat occasional pain; mild, short-term pain after surgery; or pain that occurs immediately after surgery or injury.

Swallow OxyContin Sustained-Release Tablets whole. Do NOT break, crush, chew, dissolve, or split OxyContin Sustained-Release Tablets. Doing so may cause the release of too much medicine into the bloodstream, which could be fatal.

OxyContin Sustained-Release Tablets may cause severe breathing problems. This effect may be worse if you take it with certain other medicines. Ask your doctor or pharmacist if you have questions about which medicines may add to this effect. Contact your doctor right away if you experience slow or shallow breathing.

OxyContin Sustained-Release Tablets are used for:

Treating moderate to severe pain when around-the-clock pain medicine is needed for an extended period of time.

OxyContin Sustained-Release Tablets are a narcotic (opioid) pain reliever. It works in the brain and nervous system to reduce pain.

Do NOT use OxyContin Sustained-Release Tablets if:

• you are allergic to any ingredient in OxyContin Sustained-Release Tablets


• you have known or suspected bowel blockage (eg, paralytic ileus)


• you have very slow or difficult breathing, severe asthma, or you are having an asthma attack


• you are taking sodium oxybate (GHB) or you have taken furazolidone or a monoamine oxidase inhibitor (MAOI) (eg, phenelzine) within the last 14 days


• you are taking another around-the-clock opioid pain medicine

Contact your doctor or health care provider right away if any of these apply to you.

Before using OxyContin Sustained-Release Tablets:

Some medical conditions may interact with OxyContin Sustained-Release Tablets. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding


• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement


• if you have allergies to medicines, especially other narcotic pain relievers (eg, morphine, hydromorphone); foods; or other substances


• if you have a history of asthma, chronic obstructive pulmonary disease (COPD), or other lung or breathing problems


• if you have a history of recent head injury, increased pressure in the brain, growths in the brain (eg, tumors, lesions), or seizures


• if you have a history of heart problems, low blood pressure, liver problems, kidney problems, thyroid problems, adrenal gland problems (eg, Addison disease), curvature of the spine, gallbladder problems, prostate problems, trouble urinating, or the blood disease porphyria


• if you have a history of stomach or bowel problems (eg, inflammation, blockage, esophagus or colon cancer) or surgery


• if you have difficulty swallowing, severe drowsiness, constipation, low blood oxygen levels, high blood carbon dioxide levels, low blood volume, inflammation of the pancreas, a certain type of severe or persistent diarrhea (pseudomembranous colitis), or stomach pain


• if you have a history of mood or mental problems (eg, depression, hallucinations), suicidal thoughts or behavior, drug or alcohol abuse, or if you are in alcohol or drug withdrawal


• if a member of your family has a history of mental or mood problems, or drug or alcohol abuse

Some MEDICINES MAY INTERACT with OxyContin Sustained-Release Tablets. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Azole antifungals (eg, ketoconazole), cimetidine, furazolidone, macrolide antibiotics (eg, erythromycin), MAOIs (eg, phenelzine), nefazodone, phenothiazines (eg, chlorpromazine), protease inhibitors (eg, boceprevir, ritonavir), sodium oxybate (GHB), telithromycin, or certain medicines for nausea and vomiting (eg, ondansetron) because the risk of side effects, such as severe drowsiness, slow or difficult breathing, confusion, and seizures, may be increased


• Carbamazepine, mixed narcotic agonists/antagonists (eg, buprenorphine, butorphanol, pentazocine), naltrexone, phenytoin, or rifamycins (eg, rifampin) because they may decrease OxyContin Sustained-Release Tablets's effectiveness

This may not be a complete list of all interactions that may occur. Ask your health care provider if OxyContin Sustained-Release Tablets may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use OxyContin Sustained-Release Tablets:

Use OxyContin Sustained-Release Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• OxyContin Sustained-Release Tablets comes with an extra patient information sheet called a Medication Guide. Read it carefully. Read it again each time you get OxyContin Sustained-Release Tablets refilled.


• Take OxyContin Sustained-Release Tablets by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.


• Swallow OxyContin Sustained-Release Tablets whole. Do not break, crush, chew, dissolve, or split before swallowing.


• Some patients have reported trouble swallowing OxyContin Sustained-Release Tablets. These reports have included choking, gagging, spitting tablets back up, and getting tablets stuck in the throat. To decrease these risks, take OxyContin Sustained-Release Tablets 1 tablet at a time if your dose calls for more than 1 tablet. Do not pre-soak, lick, or wet the tablet before you place it in your mouth. Take each tablet with enough water to be sure that you swallow it completely. Swallow OxyContin Sustained-Release Tablets immediately after you place it in your mouth.


• Take OxyContin Sustained-Release Tablets on a regular schedule to get the most benefit from it. It is more effective in preventing pain than in treating pain after it occurs.


• Tell your doctor if your pain gets worse or if you have breakthrough pain while taking OxyContin Sustained-Release Tablets.


• Do not suddenly stop taking OxyContin Sustained-Release Tablets. You may experience withdrawal symptoms. If you need to stop OxyContin Sustained-Release Tablets, your doctor will gradually lower your dose.


• If OxyContin Sustained-Release Tablets are no longer needed, dispose of it as soon as possible by flushing it down the toilet.


• If you miss a dose of OxyContin Sustained-Release Tablets, take it as soon as possible. Take your next dose 12 hours later. Do not take 2 doses at once. Call your doctor if you miss a dose and you are not sure what to do.

Ask your health care provider any questions you may have about how to use OxyContin Sustained-Release Tablets.

Important safety information:

• OxyContin Sustained-Release Tablets may cause dizziness, drowsiness, or changes in judgment. These effects may be worse if you take it with alcohol or certain medicines. Use OxyContin Sustained-Release Tablets with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


• Do not drink alcohol while you are taking OxyContin Sustained-Release Tablets.


• Check with your doctor before you use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are taking OxyContin Sustained-Release Tablets; they may add to OxyContin Sustained-Release Tablets's effects. Ask your pharmacist if you have questions about which medicines may cause drowsiness.


• OxyContin Sustained-Release Tablets may cause dizziness, light-headedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. To prevent them, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.


• OxyContin Sustained-Release Tablets may cause constipation. Talk with your doctor or pharmacist about using a stool softener or laxative to prevent constipation. It is also important to maintain a diet adequate in fiber, drink plenty of water, and exercise to prevent constipation. If you become constipated while taking OxyContin Sustained-Release Tablets, talk with your doctor or pharmacist.


• Do NOT take more than the prescribed dose or use for longer than prescribed without checking with your doctor.


• Tell your doctor or dentist that you take OxyContin Sustained-Release Tablets before you receive any medical or dental care, emergency care, or surgery.


• Use OxyContin Sustained-Release Tablets with caution in the ELDERLY; they may be more sensitive to its effects, especially severe breathing problems.


• OxyContin Sustained-Release Tablets should be used with extreme caution in CHILDREN younger than 18 years old; safety and effectiveness in children have not been confirmed.


• PREGNANCY AND BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using OxyContin Sustained-Release Tablets while you are pregnant. OxyContin Sustained-Release Tablets are found in breast milk. Do not breast-feed while taking OxyContin Sustained-Release Tablets.

When used for long periods of time or at high doses, OxyContin Sustained-Release Tablets may not work as well and may require higher doses to obtain the same effect as when originally taken. This is known as TOLERANCE. Talk with your doctor if OxyContin Sustained-Release Tablets stops working well. Do not take more than prescribed.

Some people who use OxyContin Sustained-Release Tablets for a long time may develop a need to continue taking it. People who take high doses are also at risk. This is known as DEPENDENCE or addiction.

Do not suddenly stop taking OxyContin Sustained-Release Tablets. If you do, you may experience WITHDRAWAL symptoms including anxiety; diarrhea; fever, runny nose, or sneezing; goose bumps and abnormal skin sensations; nausea; vomiting; pain; rigid muscles; fast or irregular heartbeat; seeing, hearing, or feeling things that are not there; shivering or tremors; sweating; and trouble sleeping.

Possible side effects of OxyContin Sustained-Release Tablets:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Constipation; dizziness; drowsiness; dry mouth; headache; nausea; sweating; vomiting; weakness.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); abnormal snoring or sighing; confusion; difficulty urinating; fainting; fast, slow, or irregular heartbeat; hallucinations; mental or mood changes; seizures; severe dizziness, drowsiness, or light-headedness; severe or persistent stomach pain, nausea, or constipation; shortness of breath; slow or shallow breathing; tremor; vision changes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: OxyContin side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include abnormal snoring; cold and clammy skin; decreased pupil size; loss of consciousness; seizures; severe drowsiness, dizziness, or lightheadedness; severe weakness; slow heartbeat; slow, shallow, or difficult breathing.

Proper storage of OxyContin Sustained-Release Tablets:

Store OxyContin Sustained-Release Tablets at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from light, heat, and moisture. Do not store in the bathroom. Keep OxyContin Sustained-Release Tablets out of the reach of children and away from pets.

General information:

• If you have any questions about OxyContin Sustained-Release Tablets, please talk with your doctor, pharmacist, or other health care provider.


• OxyContin Sustained-Release Tablets are to be used only by the patient for whom it is prescribed. Do not share it with other people.


• If your symptoms do not improve or if they become worse, check with your doctor.


• Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about OxyContin Sustained-Release Tablets. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More OxyContin resources

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

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Cabergolina Sandoz

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Cabergoline

Cabergoline is reported as an ingredient of Cabergolina Sandoz in the following countries:

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Paclitaxel is reported as an ingredient of Paclitaxel-Lans in the following countries:

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Loperamide HCl Kring

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Omnicef Suspension

Pronunciation: SEF-di-nir
Generic Name: Cefdinir
Brand Name: Omnicef

Omnicef Suspension is used for:

Treating mild to moderate infections caused by certain bacteria.

Omnicef Suspension is a cephalosporin antibiotic. It works by killing sensitive bacteria.

Do NOT use Omnicef Suspension if:

• you are allergic to any ingredient in Omnicef Suspension or any other cephalosporin antibiotic (eg, cephalexin)


• you will be receiving or have recently received a live typhoid vaccine

Contact your doctor or health care provider right away if any of these apply to you.

Before using Omnicef Suspension:

Some medical conditions may interact with Omnicef Suspension. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding


• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement


• if you have allergies to medicines, foods, or other substances


• if you have had a severe allergic reaction (eg, severe rash, hives, difficulty breathing, dizziness) to a penicillin (eg, amoxicillin) or other beta-lactam antibiotic (eg, imipenem)


• if you have a blood clotting disorder, kidney problems, seizures, diabetes, or stomach or bowel problems (eg, inflammation)

Some MEDICINES MAY INTERACT with Omnicef Suspension. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Probenecid because it may increase the risk of Omnicef Suspension's side effects


• Live typhoid vaccine because its effectiveness may be decreased by Omnicef Suspension

This may not be a complete list of all interactions that may occur. Ask your health care provider if Omnicef Suspension may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Omnicef Suspension:

Use Omnicef Suspension as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• An extra patient leaflet is available with Omnicef Suspension. Talk to your pharmacist if you have questions about this information.


• Omnicef Suspension may be taken with or without food. If stomach upset occurs, take it with food to reduce stomach irritation.


• Shake well before each use.


• Use a measuring device marked for medicine dosing. Ask your pharmacist for help if you are unsure of how to measure your dose.


• Do not take an antacid that has magnesium or aluminum in it within 2 hours before or after you take Omnicef Suspension.


• Do not take a product that has iron in it within 2 hours before or after you take Omnicef Suspension. However, you may give Omnicef Suspension along with iron-fortified infant formula.


• Omnicef Suspension works best if taken at the same times each day.


• To clear up your infection completely, take Omnicef Suspension for the full course of treatment. Keep taking it even if you feel better in a few days.


• If you miss a dose of Omnicef Suspension, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Omnicef Suspension.

Important safety information:

• Omnicef Suspension may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Omnicef Suspension with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


• Omnicef Suspension only works against bacteria; it does not treat viral infections (eg, the common cold).


• Be sure to use Omnicef Suspension for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The bacteria could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.


• Long-term or repeated use of Omnicef Suspension may cause a second infection. Tell your doctor if signs of a second infection occur. Your medicine may need to be changed to treat this.


• Contact your doctor right away if stomach pain or cramps, severe diarrhea, or bloody stools occur. Do not treat diarrhea without first checking with your doctor.


• If you are taking Omnicef Suspension and a product that contains iron, your stools may turn a reddish color. This is normal and not a cause for concern.


• Diabetes patients - Omnicef Suspension has sucrose in it. It may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.


• Diabetes patients - Omnicef Suspension may cause the results of some tests for urine ketones or glucose to be wrong. Ask your doctor before you change your diet or the dose of your diabetes medicine.


• Omnicef Suspension may interfere with certain lab tests (eg, Coomb tests). Be sure your doctor and lab personnel know you are using Omnicef Suspension.


• Use Omnicef Suspension with extreme caution in CHILDREN younger than 10 years old who have diarrhea or an infection of the stomach or bowel.


• Omnicef Suspension should be used with extreme caution in CHILDREN younger than 6 months old; safety and effectiveness in these children have not been confirmed.


• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Omnicef Suspension while you are pregnant. It is not known if Omnicef Suspension is found in breast milk. If you are or will be breast-feeding while you using Omnicef Suspension, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of Omnicef Suspension:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome: Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Diarrhea; headache; nausea.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody stools; change in the amount of urine produced; dark urine; fever, chills, or sore throat; red, swollen, blistered, or peeling skin; seizures; severe diarrhea or vomiting; severe stomach pain or cramps; unusual bleeding or bruising; vaginal irritation or discharge; yellowing of the skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Omnicef side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include diarrhea; seizures; severe nausea; stomach pain; vomiting.

Proper storage of Omnicef Suspension:

Store Omnicef Suspension at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Throw away any unused medicine after 10 days. Keep Omnicef Suspension out of the reach of children and away from pets.

General information:

• If you have any questions about Omnicef Suspension, please talk with your doctor, pharmacist, or other health care provider.


• Omnicef Suspension is to be used only by the patient for whom it is prescribed. Do not share it with other people.


• If your symptoms do not improve or if they become worse, check with your doctor.


• Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Omnicef Suspension. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Omnicef resources

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

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