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Anesthetic Adjunct Medications


Definition of Anesthetic Adjunct: Anesthetic adjuncts are used to augment specific components of anesthesia, permitting lower doses of general anesthetics with fewer side effects.

Drugs associated with Anesthetic Adjunct

The following drugs and medications are in some way related to, or used in the treatment of Anesthetic Adjunct. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.


Drug List: Brevital-Sodium Dilaudid-Hp Palladone-Extended-Release-Capsules Pentothal Stadol-Solution Sublimaze
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Wolff-Parkinson-White Syndrome Medications


Definition of Wolff-Parkinson-White Syndrome: This syndrome involves episodes of rapid heart rate (tachycardia) caused by abnormal electrical pathways (circuits) in the heart.

Drugs associated with Wolff-Parkinson-White Syndrome

The following drugs and medications are in some way related to, or used in the treatment of Wolff-Parkinson-White Syndrome. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

Learn more about Wolff-Parkinson-White Syndrome

Micromedex Care Notes:

Heart Block

Medical Encyclopedia:

Wolff-Parkinson-White syndrome
Drug List: Adenocard Adenoscan Rythmol Rythmol-Sr-Sustained-Release-Capsules Tambocor
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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: Diltia-Xt-24-Hour-Sustained-Release-Capsules Diltiazem-Hydrochloride-Sr Cartia-Xt-24-Hour-Sustained-Release-Beads-Capsules Calan-Sr-Controlled-Release-Tablets Cardizem Isoptin-Sr-Controlled-Release-Tablets Tiazac Verelan-Pm-Sustained-Release-Capsules-Controlled-Onset Diltiazem-Hydrochloride-Cd Calan Cardizem-La-24-Hour-Extended-Release-Beads-Tablets Isoptin Cardizem-Cd-24-Hour-Sustained-Release-Beads-Capsules Verelan-Sustained-Release-Pellet-Filled-Capsules Taztia-Xt-24-Hour-Extended-Release-Beads-Capsules Covera-Hs-Sustained-Release-Tablets-Controlled-Onset Dilacor-Xr-24-Hour-Sustained-Release-Capsules Dilt-Xr-24-Hour-Sustained-Release-Capsules Diltiazem-Hydrochloride-Xr Diltiazem-Hydrochloride-Xt Diltzac Matzim-La
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Atrial Fibrillation Medications


Definition of Atrial Fibrillation:

A condition where there is disorganised electrical conduction in the atria, resulting in ineffective pumping of blood into the ventricle.

Acronym: AF

Drugs associated with Atrial Fibrillation

The following drugs and medications are in some way related to, or used in the treatment of Atrial Fibrillation. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

See sub-topics

Topics under Atrial FibrillationPrevention of Thromboembolism in Atrial Fibrillation (24 drugs) Learn more about Atrial Fibrillation

Medical Encyclopedia:

Atrial fibrillation/flutter

Harvard Health Guide:

Symptoms and treatment for Atrial Fibrillation
Drug List:/tags/betapace-af/
/tags/cardizem/
/tags/cardizem-la-24-hour-extended-release-beads-tablets/
/tags/catapres/
/tags/coreg-cr-extended-release-capsules/
/tags/digitek/
/tags/dilt-xr-24-hour-sustained-release-capsules/
/tags/diltiazem-hydrochloride-cd/
/tags/diltiazem-hydrochloride-xr/
/tags/diltzac/
/tags/lanoxin/
/tags/matzim-la/
/tags/multaq/
/tags/rythmol-sr-sustained-release-capsules/
/tags/tambocor/
/tags/toprol/

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Potaba Capsules


1. Name Of The Medicinal Product

Potaba®(Potassium para-aminobenzoate)

2. Qualitative And Quantitative Composition

Capsules: white/white gelatin capsule shell containing the active ingredient 500mg of potassium para-aminobenzoate powder.

3. Pharmaceutical Form

Capsules: White/white size zero gelatin capsules containing 500mg potassium para-aminobenzoate with Potaba 51 on the shell.

4. Clinical Particulars 4.1 Therapeutic Indications

Peyronie's Disease

Scleroderma

4.2 Posology And Method Of Administration

Potaba capsules should be taken orally; six capsules four times daily with food.

Children: not recommended.

4.3 Contraindications

Potaba should not be given to patients taking sulphonamides as it will inactivate this medication.

4.4 Special Warnings And Precautions For Use

Treatment with Potaba should be interrupted during periods of low food intake (egg, during fasting, anorexia, nausea). This is to avoid the possible development of hypoglycaemia.

Potaba treatment should be given cautiously to patients with renal impairment and treatment discontinued if a hypersensitivity reaction occurs.

Potaba should not be taken by patients on sulphonamides; Potaba may cause inactivation of this medication.

4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction

With the exception of sulphonamides, no interactions with other medicaments have been established.

4.6 Pregnancy And Lactation

No information is available on this, therefore it is not recommended.

4.7 Effects On Ability To Drive And Use Machines

There is no evidence that Potaba has any effect on ability to drive or use machines.

4.8 Undesirable Effects

Treatment with Potaba should be interrupted during periods of low food intake,(e.g. during fasting, anorexia, nausea).This is to avoid the possible development of hypoglycaemia.

No serious adverse effects have been reported in patients treated with Potaba.

4.9 Overdose

No particular problems are expected following overdosage with Potaba. Symptomatic and supportive therapy should be given as appropriate.

5. Pharmacological Properties 5.1 Pharmacodynamic Properties

P.Aminobenzoate is considered a member of the Vitamin B complex. Small amounts are found in cereal, eggs, milk and meats. Detectable amounts are normally present in human blood, spinal fluid, urine and sweat. The pharmacological action of this chemical has not been clearly established, but it has been suggested that the antifibrosis activity of Potaba is brought about by the drug increasing oxygen uptake at the tissue level. Fibrosis is believed to occur from either too much serotonin or too little monoamine oxidase activity over a period of time. The activity of monoamine oxidase is dependant on an adequate oxygen supply. By increasing oxygen supply at tissue level Potaba enhances monoamine oxidase activity thereby preventing or bringing about regression of fibrosis.

5.2 Pharmacokinetic Properties

Potaba is rapidly absorbed and metabolised as food. Excretion is through renal function.

5.3 Preclinical Safety Data

N/A

6. Pharmaceutical Particulars 6.1 List Of Excipients

None

6.2 Incompatibilities

Sulphonamides.

6.3 Shelf Life

Capsules: three years from date of manufacture.

6.4 Special Precautions For Storage

Store below 25?C.

6.5 Nature And Contents Of Container

.

White polypropylene tube with tamper-evident polyethylene cap. A filla may be inserted to reduce ullage.

Containers of 240 x 500mg capsules.

6.6 Special Precautions For Disposal And Other Handling 7. Marketing Authorisation Holder

Glenwood Laboratories Ltd. ,

Jenkins Dale,

Chatham

Kent ME4 5RD

8. Marketing Authorisation Number(S)

Potaba Capsules: 00245/5001R

9. Date Of First Authorisation/Renewal Of The Authorisation

March 1998

10. Date Of Revision Of The Text

June 2002


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Vulvodynia Medications


Definition of Vulvodynia: Vulvodynia is described as chronic vulvar discomfort with complaints of burning and superficial irritation.

Drugs associated with Vulvodynia

The following drugs and medications are in some way related to, or used in the treatment of Vulvodynia. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.


Drug List: Aventyl Carbatrol-Sustained-Release-Capsules Effexor-Xr-Extended-Release-Capsules Elavil Epitol Fanatrex Gabarone Lexapro Neurontin Norpramin Pamelor Prozac Prozac-Weekly-Delayed-Release-Capsules Rapiflux Tegretol Tegretol-Xr-Sustained-Release-Tablets Topamax Topamax-Sprinkle Topiragen Vanatrip
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Nabilone 1mg Capsules


Nabilone 1 mg Capsules

(nabilone)

Read all of this leaflet carefully before you start taking this medicine. Keep this leaflet. You may need to read it again. If you have any further questions, ask your doctor or pharmacist. This medicine has been prescribed for you. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours. If you experience any side effect and this becomes serious, tell your doctor or pharmacist. In this leaflet: 1. What Nabilone is and what it is used for 2. Before you take Nabilone Capsules 3. How to take Nabilone Capsules 4. Possible side effects 5. How to store Nabilone Capsules 6. Further information What Nabilone Is And What It Is Used For

Nabilone is a medicine that helps to reduce nausea and vomiting caused by many anticancer medicines.

Nabilone is often used when other medicines have not helped your nausea or vomiting.

Nabilone is a man-made chemical known as a cannabinoid. It is not made from the Cannabis plant but it is similar to some marijuana extracts and can cause similar effects.

Before You Take Nabilone Capsules Do not take Nabilone If you are allergic (hypersensitive) to any of the other ingredients of Nabilone Capsules (these are listed in section 6, "Further Information"). If your nausea / vomiting is not due to anticancer treatment. If you are under 18 years. Nabilone is not meant for children. Take special care with Nabilone

It is best if you take Nabilone Capsules in hospital, as you may experience side effects.

Tell your doctor before you start treatment if you have any of the following problems or if you develop any of these during treatment:

Any liver problems. High blood pressure or any other heart problem. Any mental illness, for example depression or schizophrenia. Taking other medicines

Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription.

In particular, tell your doctor if you are taking any sleeping pills, pain killers or tranquillisers.

Taking Nabilone with alcohol

Do not drink alcohol while you are taking Nabilone.

Pregnancy and breast-feeding

Tell your doctor before you start treatment

If you are pregnant, if you think that you are pregnant, or if you intend to become pregnant. If you are breast-feeding or planning to breast-feed.

Your doctor will then decide if you can take this medicine.

Driving and using machines

Nabilone Capsules may cause side effects such as sleepiness, confusion, hallucinations, a feeling of dizziness or spinning, poor muscle co-ordination, problems with your sight and problems with concentration. These side effects may occur up to 3 days after taking Nabilone. This may affect your ability to drive and operate machinery. Do not drive or operate machinery if you experience any of these side effects.

How To Take Nabilone Capsules

Always take Nabilone exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure how to take it. Your doctor will usually start you on the lowest possible dose.

It is best if you take Nabilone Capsules in hospital, especially the first time that you take Nabilone. This is because you may experience side effects.

The hospital doctor or nurse may give you your first dose the night before you start chemotherapy and the second dose one to three hours before it begins.

Swallow the capsules with water.

Dose The usual dose is 1 or 2 capsules twice a day. You should never take more than 2 capsules three times a day. You can take Nabilone while you are having chemotherapy treatment and for up to 2 days after your last dose of chemotherapy.

The dosing recommendations for elderly patients are the same as for other adults.

If you take more Nabilone than you should

If you ever take too many capsules, tell your doctor or get someone to take you to the nearest hospital casualty department immediately together with your medicine to show to the doctor.

If you forget to take Nabilone

If you miss a dose, wait until it is time for the next dose, and then continue as before.

Do not take a double dose to make up for a forgotten dose.

Possible Side Effects

Like all medicines, Nabilone can cause side effects, although not everybody gets them.

Side effects that you may experience are: Feeling sleepy, relaxed, or "high". A few patients have had hallucinations, felt confused, depressed, anxious or had other changes in their mood or mental state. A feeling of dizziness or spinning, especially when you stand up. Poor muscle co-ordination. Dry mouth, problems with your sight or concentration, difficulty sleeping, or headaches. Shaking, a faster heart beat than normal, low blood pressure, losing your appetite and stomach pains.

Any changes in your mood, such as feeling depressed, relaxed or "high", may last for 2 or 3 days after you stop taking Nabilone. You may find that you get used to these feelings.

If you have any of these side effects, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

How To Store Nabilone Capsules Keep Nabilone Capsules out of the reach and sight of children. Do not use Nabilone after the expiry date which is stated on the bottle and carton after "EXP". The expiry date refers to the last day of that month. Keep the container tightly closed. Store your capsules at room temperature (15-25°C) in a dry place. If your doctor tells you to stop taking the capsules, please take them back to the pharmacist. Medicines should not be disposed of via wastewater or household waste. Only keep the capsules if your doctor tells you to. Further Information What Nabilone contains

Active substance: Nabilone. Each capsule contains 1 mg of nabilone.
Other ingredients: Povidone, starch, gelatin and the colourants E132, E172 and E171.

What Nabilone looks like and contents of the pack Nabilone capsules are blue and white and have CL 3101 printed on them. Each bottle or blister pack of Nabilone contains 20 capsules. Marketing Authorisation Holder Meda Pharmaceuticals Ltd. Skyway House Parsonage Road Takeley Bishop's Stortford CM22 6PU UK Manufacturer Dales Pharmaceuticals Limited Snaygill Industrial Estate Keighley Road Skipton North Yorkshire BD23 2RW UK

For any information about this medicine, please contact the Marketing Authorisation Holder.

This leaflet was last approved in July 2009.

F687


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Fibromyalgia Medications


Drugs associated with Fibromyalgia

The following drugs and medications are in some way related to, or used in the treatment of Fibromyalgia. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

See sub-topics

Topics under Fibromyalgia Epicondylitis, Tennis Elbow (17 drugs) Learn more about Fibromyalgia

Medical Encyclopedia:

Fibromyalgia

Harvard Health Guide:

Symptoms and treatment for Fibromyalgia

Drugs.com Health Center:

Fibromyalgia
Drug List: 5-Htp Amibid-La Amrix-Extended-Release-Capsules Comfort-Pac-With-Cyclobenzaprine Cymbalta Deltasone Desyrel Desyrel-Dividose Effexor Effexor-Xr-Extended-Release-Capsules Elavil Fanatrex Fexmid Flexeril Gabarone Ganidin-Nr Gg-200-Nr Guaifenesin-La Guaifenex-G Guaifenex-La Lexapro Lyrica Meticorten Mobic Mucinex Muco-Fen-1200 Neurontin Nuvigil Organidin-Nr-Immediate-Release-Capsules Pristiq Prozac Prozac-Weekly-Delayed-Release-Capsules Q-Bid-La Rapiflux Revia Savella Skelaxin Sterapred Sterapred-Ds Strattera Topamax Topamax-Sprinkle Topiragen Vanatrip Xyrem
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Calcium channel 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.

Calcium channel blockers block voltage gated calcium channels and inhibits the influx of calcium ions into cardiac and smooth muscle cells. The decrease in intracellular calcium reduces the strength of heart muscle contraction, reduces conduction of impulses in the heart, and causes vasodilatation.

Decrease in intracellular calcium in the heart decreases cardiac contractility. Decreased calcium in the vascular smooth muscle reduces its contraction and therefore causes vasodilatation.

Decrease in cardiac contractility decreases cardiac output and vasodilatation decreases total peripheral resistance, both of which cause a drop in blood pressure.

Calcium channel blocking agents are used to treat hypertension.

See also

Medical conditions associated with calcium channel blocking agents:

Angina Angina Pectoris Prophylaxis Arrhythmia Atrial Fibrillation Atrial Flutter Bipolar Disorder Cluster Headaches Coronary Artery Disease Heart Failure High Blood Pressure Hypertensive Emergency Hypertrophic Cardiomyopathy Idiopathic Hypertrophic Subaortic Stenosis Ischemic Stroke Migraine Prevention Nocturnal Leg Cramps Premature Labor Raynaud's Syndrome Subarachnoid Hemorrhage Supraventricular Tachycardia Drug List: Afeditab-Cr Diltia-Xt-24-Hour-Sustained-Release-Capsules Diltiazem-Hydrochloride-Sr Nimotop Adalat Cartia-Xt-24-Hour-Sustained-Release-Beads-Capsules Calan-Sr-Controlled-Release-Tablets Cardizem Isoptin-Sr-Controlled-Release-Tablets Nifediac-Cc Tiazac Verelan-Pm-Sustained-Release-Capsules-Controlled-Onset Diltiazem-Hydrochloride-Cd Procardia Adalat-Cc-Sustained-Release-Tablets Calan Cardizem-La-24-Hour-Extended-Release-Beads-Tablets Procardia-Xl-Sustained-Release-Tablets Isoptin Nifedical-Xl Cardizem-Cd-24-Hour-Sustained-Release-Beads-Capsules Norvasc Plendil Dynacirc-Cr-Extended-Release-Tablets Verelan-Sustained-Release-Pellet-Filled-Capsules Taztia-Xt-24-Hour-Extended-Release-Beads-Capsules Cardene Cardene-Iv Cardene-Sr-Sustained-Release-Capsules Cleviprex Covera-Hs-Sustained-Release-Tablets-Controlled-Onset Dilacor-Xr-24-Hour-Sustained-Release-Capsules Dilt-Xr-24-Hour-Sustained-Release-Capsules Diltiazem-Hydrochloride-Xr Diltiazem-Hydrochloride-Xt Diltzac Dynacirc Matzim-La Sular-Extended-Release-Tablets Vascor
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Migraine Prevention (Migraine Prophylaxis) Medications



Hydrocephalus Medications


Definition of Hydrocephalus: Hydrocephalus is an accumulation of cerebrospinal fluid in the ventricles of the brain, leading to their enlargement and swelling.

Drugs associated with Hydrocephalus

The following drugs and medications are in some way related to, or used in the treatment of Hydrocephalus. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

Learn more about Hydrocephalus

Micromedex Care Notes:

Hydrocephalus Hydrocephalus In Children

Medical Encyclopedia:

Hydrocephalus

Harvard Health Guide:

Symptoms and treatment for Hydrocephalus
Drug List: Diamox Diamox-Sequels-Sustained-Release-Capsules
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Cevi-Bid Controlled-Release Capsules


Pronunciation: a-SKOR-bik AS-id
Generic Name: Ascorbic Acid
Brand Name: Examples include Cemill and Cevi-Bid
Cevi-Bid Controlled-Release Capsules are used for:

Treating and preventing low levels of vitamin C. It may also be used for other conditions as determined by your doctor.

Cevi-Bid Controlled-Release Capsules are a vitamin. It works by supplementing vitamin C, which is used in many functions in the body.

Do NOT use Cevi-Bid Controlled-Release Capsules if: you are allergic to any ingredient in Cevi-Bid Controlled-Release Capsules

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

Before using Cevi-Bid Controlled-Release Capsules:

Some medical conditions may interact with Cevi-Bid Controlled-Release Capsules. 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 diabetes, glucose-6-phosphate dehydrogenase deficiency, a high iron level in the blood, anemia (eg, sickle cell, sideroblastic, thalassemia), or kidney stones

Some MEDICINES MAY INTERACT with Cevi-Bid Controlled-Release Capsules. Tell your health care provider if you are taking any other medicines, especially any of the following:

Anticoagulants (eg, warfarin) because side effects may be increased by Cevi-Bid Controlled-Release Capsules

This may not be a complete list of all interactions that may occur. Ask your health care provider if Cevi-Bid Controlled-Release Capsules 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 Cevi-Bid Controlled-Release Capsules:

Use Cevi-Bid Controlled-Release Capsules as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Cevi-Bid Controlled-Release Capsules may be taken with or without food. Swallow Cevi-Bid Controlled-Release Capsules whole. Do not break, crush, or chew before swallowing. Take Cevi-Bid Controlled-Release Capsules with a full glass of water (8 oz/240 mL). Do not lie down for 30 minutes after taking Cevi-Bid Controlled-Release Capsules. If you miss a dose of Cevi-Bid Controlled-Release Capsules, 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 Cevi-Bid Controlled-Release Capsules.

Important safety information: Do not take large doses of vitamins (megadoses or megavitamin therapy) while taking Cevi-Bid Controlled-Release Capsules unless directed to by your doctor. Cevi-Bid Controlled-Release Capsules may cause incorrect results with some in-home cholesterol test kits. Check with your doctor or pharmacist if you are taking Cevi-Bid Controlled-Release Capsules and need to check your cholesterol at home. Diabetes patients - Cevi-Bid Controlled-Release Capsules may cause incorrect test results with some urine glucose tests. Check with your doctor before you adjust the dose of your diabetes medicine or change your diet. Cevi-Bid Controlled-Release Capsules may cause incorrect test results with kits used to check for blood in the stool. Check with your doctor if you are taking Cevi-Bid Controlled-Release Capsules when using the test kit. PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Cevi-Bid Controlled-Release Capsules, discuss with your doctor the benefits and risks of using Cevi-Bid Controlled-Release Capsules during pregnancy. Cevi-Bid Controlled-Release Capsules are excreted in breast milk. If you are or will be breast-feeding while you are using Cevi-Bid Controlled-Release Capsules, check with your doctor or pharmacist to discuss the risks to your baby. Possible side effects of Cevi-Bid Controlled-Release Capsules:

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:

Diarrhea; nausea; upset stomach; vomiting.

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

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); kidney stones (eg, abdominal pain/back pain, painful urination).

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: Cevi-Bid 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 gout.

Proper storage of Cevi-Bid Controlled-Release Capsules:

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

General information: If you have any questions about Cevi-Bid Controlled-Release Capsules, please talk with your doctor, pharmacist, or other health care provider. Cevi-Bid Controlled-Release Capsules 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 Cevi-Bid Controlled-Release Capsules. 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 Cevi-Bid resources Cevi-Bid Side Effects (in more detail) Cevi-Bid Use in Pregnancy & Breastfeeding Cevi-Bid Drug Interactions Cevi-Bid Support Group 0 Reviews for Cevi-Bid - Add your own review/rating Compare Cevi-Bid with other medications Dietary Supplementation Scurvy Urinary Acidification
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Boots Paracetamol 500 mg Capsules (P -32)


Boots Paracetamol 500 mg Capsules

Read all of this leaflet carefully because it contains important information for you.

This medicine is available without prescription to treat minor conditions. However, you still need to take it carefully to get the best results from it.

Keep this leaflet, you may need to read it again Ask your pharmacist if you need more information or advice What this medicine is for

This medicine contains a painkiller to relieve mild to moderate pain and fever.

It can be used to relieve headaches, migraine, rheumatic aches and pains, muscular pain and back pain, neuralgia, toothache, sore throat, period pain, fever and the symptoms of colds and flu.

Before you take this medicine

This medicine can be taken by adults and children aged 12 years and over. However, some people should not take this medicine or should seek the advice of their pharmacist or doctor first.

Do not take: If you are allergic to any of the ingredients Talk to your pharmacist or doctor: If you have severe kidney problems or severe liver problems (including a disease caused by drinking alcohol) If you are pregnant

You can take this medicine if you are breastfeeding.

Other important information

Information about some of the ingredients: Propyl parahydroxybenzoate (E216) and methyl parahydroxybenzoate (E218) in this medicine may cause allergic reactions (possibly delayed).

If you take other medicines

This medicine contains paracetamol.

Do not take with any other paracetamol-containing products.

Before you take these capsules, make sure that you tell your pharmacist about ANY other medicines you might be using at the same time, particularly the following:

Metoclopramide or domperidone (for feeling sick or being sick) Colestyramine (to reduce blood fat levels) Warfarin or other blood thinners - If you take warfarin you can take occasional amounts of this medicine, but talk to your doctor first before you take it on a regular basis

If you are unsure about interactions with any other medicines, talk to your pharmacist. This includes medicines prescribed by your doctor and medicine you have bought for yourself, including herbal and homeopathic remedies.

How to take this medicine

Check the foil is not broken before use. If it is, do not take that capsule.

Adults and children of 12 years and over: Take one or two capsules three or four times a day, if you need to.
Don’t take more than 8 capsules in any 24 hours. Don’t take more often than every 4 hours.

Swallow each capsule with water.

Do not give to children under 12 years.

Do not take more than the amount recommended above.

If symptoms do not go away talk to your doctor.

If you take too many capsules: Immediate medical advice should be sought in the event of an overdose, even if you feel well, because of the risk of delayed, serious liver damage. Go to your nearest hospital casualty department. Take your medicine and this leaflet with you.

Possible side effects

Most people will not have problems, but some may get some.

If you get any of these serious side effects, stop taking the capsules. See a doctor at once: Difficulty in breathing, swelling of the face, neck, tongue or throat (severe allergic reactions) These other effects are less serious. If they bother you talk to a pharmacist: Skin rash Unusual bruising, or infections such as sore throats - this may be a sign of very rare changes in the blood

If any side effect becomes severe, or you notice any side effect not listed here, please tell your pharmacist or doctor.

How to store this medicine

Do not store above 25°C.

Store in the original package.

Keep this medicine in a safe place out of the sight and reach of children, preferably in a locked cupboard.

Use by the date on the end flap of the carton.

What is in this medicine

Each hard gelatin capsule contains Paracetamol 500 mg, which is the active ingredient.

As well as the active ingredient, the capsules also contain pregelatinised maize starch, magnesium stearate, sodium laurilsulfate. The capsule shell contains titanium dioxide (E171), erythrosine (E127), quinoline yellow (E104), Patent Blue V (E131), gelatin, methyl parahydroxybenzoate (E218), propyl parahydroxybenzoate (E216).

The pack contains 32 hard gelatin capsules with a red cap and white body.

Who makes this medicine

Manufactured for

The Boots Company PLC Nottingham NG2 3AA

by the Marketing Authorisation holder

Bristol Laboratories Ltd Unit 3 Canalside Northbridge Road Berkhamsted Hertfordshire HP4 1EG

Leaflet prepared July 2007

If you would like any further information about this medicine, please contact

The Boots Company PLC Nottingham NG2 3AA

3448-32eMC-Xpil


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Proton pump 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.

Proton pump inhibitors act by irreversible inhibition of the H+/K+ ATPase, in the parietal cells of the stomach. It markedly inhibits gastric acid secretion and has a long duration of action. They are used for treatment of gastric and duodenal ulcers, gastroesophageal reflux disease and other excessive gastrointestinal acid secretory disorders.

See also

Medical conditions associated with proton pump inhibitors:

Aspiration PneumoniaBarrett's EsophagusDuodenal UlcerDuodenal Ulcer ProphylaxisErosive EsophagitisGastrointestinal HemorrhageGERDHelicobacter Pylori InfectionIndigestionMultiple Endocrine AdenomasNSAID-Induced Gastric UlcerNSAID-Induced Ulcer ProphylaxisPathological Hypersecretory ConditionsPeptic UlcerStomach UlcerStress Ulcer ProphylaxisSystemic MastocytosisZollinger-Ellison Syndrome Drug List:/tags/zegerid/
/tags/nexium_iv/
/tags/prevacid/
/tags/kapidex/
/tags/prilosec/
/tags/prevacid-solutab-orally-disintegrating-tablets/
/tags/prevacid-i-v/
Protonix-I-V
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Bartter Syndrome Medications


Definition of Bartter Syndrome: Bartter syndrome refers to a rare group of conditions that affect the kidneys. People with Bartter syndrome have a loss of potassium (hypokalemic alkalosis) and a rise in the hormone aldosterone.

Drugs associated with Bartter Syndrome

The following drugs and medications are in some way related to, or used in the treatment of Bartter Syndrome. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

Topics under Bartter Syndrome Gitelman Syndrome (3 drugs) Learn more about Bartter Syndrome

Medical Encyclopedia:

Bartter syndrome
Drug List: Indocin Indocin-Iv Indocin-Sr-Sustained-Release-Capsules
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Methylxanthines


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.

Methylxanthines act as bronchodilators by relaxing bronchial smooth muscle and helps the constricted airways to dilate. The exact mechanism of action with regards to methylxanthine causing bronchodilatation is not well understood but it appears that methylxanthines inhibit the enzyme phosphodiesterase, which degrades cyclic AMP, so methylxanthines tend to increase the concentration of cyclic AMP.

Methylxanthines are bronchodilators used in the treatment of asthma and chronic obstructive pulmonary disease (COPD).

See also

Medical conditions associated with methylxanthines:

Apnea of Prematurity Asthma Asthma, acute Asthma, Maintenance Bronchitis COPD Drug List: Theo-24-Sustained-Release-Capsules Uniphyl-Sustained-Release-Tablets Theo-Dur Choledyl Choledyl-Sa Dilor Dilor-400 Dylix-Elixir Elixophyllin-Elixir Lufyllin Lufyllin-400 Neothylline Phyllocontin Quibron-T Quibron-T-Sr Theo-Time Theocap-Sustained-Release-Capsules Theochron-Sustained-Release-Tablets Theolair-Tablets Truphylline Truxophyllin
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Carbetapentane/Guaifenesin Sustained-Release Capsules


Pronunciation: car-bay-ta-PEN-tane/gwye-FEN-eh-sin
Generic Name: Carbetapentane/Guaifenesin
Brand Name: Dynex VR
Carbetapentane/Guaifenesin Sustained-Release Capsules are used for:

Relieving unproductive cough and reducing mucus in the chest due to colds, flu, or hay fever. It may also be used for other conditions as determined by your doctor.

Carbetapentane/Guaifenesin Sustained-Release Capsules are a cough suppressant and expectorant combination. The cough suppressant works in the brain to help decrease the cough reflex. The expectorant works by thinning mucus (phlegm) in the lungs, making it less sticky and easier to cough up. This makes coughs more productive.

Do NOT use Carbetapentane/Guaifenesin Sustained-Release Capsules if: you are allergic to any ingredient in Carbetapentane/Guaifenesin Sustained-Release Capsules

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

Before using Carbetapentane/Guaifenesin Sustained-Release Capsules:

Some medical conditions may interact with Carbetapentane/Guaifenesin Sustained-Release Capsules. 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 chronic cough due to smoking, asthma, chronic bronchitis, or emphysema, or if your cough produces large amounts of mucus if you have a history of heart problems, high blood pressure, prostate problems, an overactive thyroid, diabetes, or glaucoma

Some MEDICINES MAY INTERACT with Carbetapentane/Guaifenesin Sustained-Release Capsules. Tell your health care provider if you are taking any other medicines. However, no specific interactions with Carbetapentane/Guaifenesin Sustained-Release Capsules are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Carbetapentane/Guaifenesin Sustained-Release Capsules 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 Carbetapentane/Guaifenesin Sustained-Release Capsules:

Use Carbetapentane/Guaifenesin Sustained-Release Capsules as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Carbetapentane/Guaifenesin Sustained-Release Capsules may be taken with or without food. Drinking extra fluids while you are taking Carbetapentane/Guaifenesin Sustained-Release Capsules are recommended. Check with your doctor for instructions. Swallow Carbetapentane/Guaifenesin Sustained-Release Capsules whole. Do not break, crush, or chew before swallowing. If you miss a dose of Carbetapentane/Guaifenesin Sustained-Release Capsules and you are taking it regularly, 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 Carbetapentane/Guaifenesin Sustained-Release Capsules.

Important safety information: Carbetapentane/Guaifenesin Sustained-Release Capsules may cause drowsiness. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Carbetapentane/Guaifenesin Sustained-Release Capsules. Using Carbetapentane/Guaifenesin Sustained-Release Capsules alone, with certain other medicines, or with alcohol may lessen your ability to drive or perform other potentially dangerous tasks. Avoid drinking alcohol or taking other medications that cause drowsiness (eg, sedatives, tranquilizers) while taking Carbetapentane/Guaifenesin Sustained-Release Capsules. Carbetapentane/Guaifenesin Sustained-Release Capsules will add to the effects of alcohol and other depressants. Ask your pharmacist if you have questions about which medicines are depressants. If cough persists for more than 1 week or is accompanied by a fever, contact your health care provider. A persistent cough could be a sign of a serious condition. Carbetapentane/Guaifenesin Sustained-Release Capsules are not recommended for use in CHILDREN younger than 6 years of age. Safety and effectiveness in this age group have not been confirmed. PREGNANCY and BREAST-FEEDING: If you become pregnant, discuss with your doctor the benefits and risks of using Carbetapentane/Guaifenesin Sustained-Release Capsules during pregnancy. It is unknown if Carbetapentane/Guaifenesin Sustained-Release Capsules are excreted in breast milk. If you are or will be breast-feeding while you are using Carbetapentane/Guaifenesin Sustained-Release Capsules, check with your doctor or pharmacist to discuss the risks to your baby. Possible side effects of Carbetapentane/Guaifenesin Sustained-Release Capsules:

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:

Drowsiness; dry mouth, nose, or throat; upset stomach.

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

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).

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: Carbetapentane/Guaifenesin 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 restlessness; seizures; severe agitation.

Proper storage of Carbetapentane/Guaifenesin Sustained-Release Capsules:

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

General information: If you have any questions about Carbetapentane/Guaifenesin Sustained-Release Capsules, please talk with your doctor, pharmacist, or other health care provider. Carbetapentane/Guaifenesin Sustained-Release Capsules 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 Carbetapentane/Guaifenesin Sustained-Release Capsules. 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 Carbetapentane/Guaifenesin resources Carbetapentane/Guaifenesin Side Effects (in more detail) Carbetapentane/Guaifenesin Use in Pregnancy & Breastfeeding Carbetapentane/Guaifenesin Drug Interactions Carbetapentane/Guaifenesin Support Group 0 Reviews for Carbetapentane/Guaifenesin - Add your own review/rating Compare Carbetapentane/Guaifenesin with other medications Cough
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Bartonellosis Medications


Definition of Bartonellosis: Cat scratch disease is an infectious illness caused by the bacteria More...

Drugs associated with Bartonellosis

The following drugs and medications are in some way related to, or used in the treatment of Bartonellosis. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

Learn more about Bartonellosis

Medical Encyclopedia:

Cat scratch disease
Drug List: Azithromycin-3-Day-Dose-Pack Doryx-Delayed-Release-Capsules Doxy-100 Doxy-200 E-E-S-Granules-Suspension E-E-S-200 E-E-S-400 E-E-S-400-Filmtab Ery-Tab Eryc-Delayed-Release-Particles-Capsules Eryped-Drops Erythrocin Erythromycin-Lactobionate-I-V Erythrocin-Stearate-Filmtab Ilosone Monodox Ocudox-Convenience-Kit Oraxyl Pce Rifadin Rifadin-Iv Rimactane Vibra-Tabs Vibramycin Zithromax Zmax-Extended-Release-Oral-Suspension
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ADHD (Attention Deficit Hyperactivity Disorder) Medications


Definition of ADHD: An inability to control behaviour due to difficulty in processing neural stimuli. More...

Drugs associated with ADHD

The following drugs and medications are in some way related to, or used in the treatment of ADHD. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

See sub-topics

Topics under ADHD Oppositional Defiant Disorder (1 drug) Learn more about ADHD (Attention Deficit Hyperactivity Disorder)

Medical Encyclopedia:

Attention deficit hyperactivity disorder (ADHD)

Drugs.com Health Center:

Mental Health Disorders
Drug List: 5-Htp Adderall Adderall-Xr-Extended-Release-Capsules Aminomine Animi-3 Animi-3-With-Vitamin-D Concerta Cylert Daytrana Desoxyn Desoxyn-Gradumet Dexedrine Dextrostat Divista Eldepryl Epa-Fish-Oil Fish_Oil Fish-Oil-Ultra Focalin Focalin-Xr-Extended-Release-Capsules Icar-Prenatal-Essential-Omega-3 Intuniv Kapvay Liquadd-Solution Lovaza Marine-Lipid-Concentrate Maxepa Maxitears-Dry-Eye-Formula Maxivision-Omega-3-Formula Metadate-Cd-Controlled-Release-Capsules Metadate-Er Methylin Methylin-Er-Controlled-Release-Tablets Mi-Omega Mi-Omega-Nf Norpramin Omacor Omega-500 Pristiq Procentra-Solution Proepa Ritalin Ritalin-La-Extended-Release-Capsules Ritalin-Sr-Controlled-Release-Tablets Sea-Omega Sea-Omega-30 Sea-Omega-70 Strattera Theratears-Nutrition Theromega Tofranil Tofranil-Pm Vyvanse Zelapar
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Typhoid Vaccine Delayed-Release Capsules


Pronunciation: TIE-foyd
Generic Name: Typhoid Vaccine Live
Brand Name: Vivotif Berna Vaccine
Typhoid Vaccine Delayed-Release Capsules are used for:

Preventing typhoid fever in persons 6 years old and older who are at increased risk because they are traveling to an area where this infection is more common, have been in contact with infected individuals, or work in an environment that increases their risk (eg, lab work).

Typhoid Vaccine Delayed-Release Capsules are a vaccine. It works by stimulating the body to produce antibodies against typhoid fever.

Do NOT use Typhoid Vaccine Delayed-Release Capsules if: you are allergic to any ingredient in Typhoid Vaccine Delayed-Release Capsules you have a current infection, cancer, fever, persistent vomiting or diarrhea, other stomach illness, or HIV or another condition that weakens the immune system you are taking a sulfonamide (eg, sulfamethoxazole), another antibiotic (eg, penicillin), or a medicine that weakens the immune system (eg, cyclosporine, certain cancer medicines)

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

Before using Typhoid Vaccine Delayed-Release Capsules:

Some medical conditions may interact with Typhoid Vaccine Delayed-Release Capsules. 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 an infection or fever, chronic diarrhea, an illness affecting the stomach or intestines, undiagnosed rectal hemorrhage, or persistent vomiting, or you are receiving chemotherapy or radiation therapy

Some MEDICINES MAY INTERACT with Typhoid Vaccine Delayed-Release Capsules. Tell your health care provider if you are taking any other medicines, especially any of the following:

Antibiotics (eg, penicillin), corticosteroids (eg, prednisone), immunosuppressants (eg, certain cancer medicines, cyclosporine), or sulfonamides (eg, sulfamethoxazole) because they may decrease Typhoid Vaccine Delayed-Release Capsules's effectiveness Proguanil because it may decrease Typhoid Vaccine Delayed-Release Capsules's effectiveness. You should not take proguanil for at least 10 days after your last dose of Typhoid Vaccine Delayed-Release Capsules. Discuss any questions with your doctor

This may not be a complete list of all interactions that may occur. Ask your health care provider if Typhoid Vaccine Delayed-Release Capsules 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 Typhoid Vaccine Delayed-Release Capsules:

Use Typhoid Vaccine Delayed-Release Capsules as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Take Typhoid Vaccine Delayed-Release Capsules with a cold or lukewarm drink 1 hour before or 2 hours after a meal. Swallow Typhoid Vaccine Delayed-Release Capsules whole. Do not break, crush, or chew before swallowing. Do not take cracked or broken capsules. Do not drink alcohol within 2 hours of taking Typhoid Vaccine Delayed-Release Capsules. Do not forget to skip a day between capsules. Take a capsule EVERY OTHER DAY as directed by your doctor. For Typhoid Vaccine Delayed-Release Capsules to be effective, you must complete all 4 doses at least 1 week before exposure to typhoid fever. If you miss a dose of Typhoid Vaccine Delayed-Release Capsules, take it as soon as possible. If you do not remember until the next day, take the dose as soon as possible and reschedule your doses from that day.

Ask your health care provider any questions you may have about how to use Typhoid Vaccine Delayed-Release Capsules.

Important safety information: Notify your doctor if you experience diarrhea, vomiting, or flu-like symptoms after taking Typhoid Vaccine Delayed-Release Capsules. This vaccine helps prevent typhoid fever, but does not provide 100% protection. It is important to also avoid infected people, food, and water. It is recommended that you receive another 4 doses of Typhoid Vaccine Delayed-Release Capsules every 5 years if you continue to be exposed to typhoid fever. Typhoid Vaccine Delayed-Release Capsules are not recommended for use in CHILDREN younger than 6 years of age; 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 Typhoid Vaccine Delayed-Release Capsules during pregnancy. It is not known if Typhoid Vaccine Delayed-Release Capsules are found in breast milk. If you are or will be breast-feeding while you use Typhoid Vaccine Delayed-Release Capsules, check with your doctor. Discuss any possible risks to your baby. Possible side effects of Typhoid Vaccine Delayed-Release Capsules:

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:

Diarrhea; fever; headache; muscle pain; nausea; stomach cramps or pain; vomiting.

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); difficulty swallowing; unusual hoarseness.

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: Typhoid 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.

Proper storage of Typhoid Vaccine Delayed-Release Capsules:

Store Typhoid Vaccine Delayed-Release Capsules in the refrigerator, between 36 and 46 degrees F (2 and 8 degrees C), at all times. Do not freeze. Keep Typhoid Vaccine Delayed-Release Capsules out of the reach of children and away from pets.

General information: If you have any questions about Typhoid Vaccine Delayed-Release Capsules, please talk with your doctor, pharmacist, or other health care provider. Typhoid Vaccine Delayed-Release Capsules 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 Typhoid Vaccine Delayed-Release Capsules. 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 Typhoid Vaccine resources Typhoid Vaccine Side Effects (in more detail) Typhoid Vaccine Dosage Typhoid Vaccine Use in Pregnancy & Breastfeeding Typhoid Vaccine Drug Interactions Typhoid Vaccine Support Group 0 Reviews for Typhoid - Add your own review/rating Compare Typhoid Vaccine with other medications Typhoid Prophylaxis
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