Monday, 26 September 2016

Azasite Drops


Pronunciation: ay-ZITH-roe-MYE-sin
Generic Name: Azithromycin
Brand Name: Azasite


Azasite Drops are used for:

Treating eye infections caused by certain bacteria.


Azasite Drops are a macrolide antibiotic. It works by killing sensitive bacteria.


Do NOT use Azasite Drops if:


  • you are allergic to any ingredient in Azasite Drops

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



Before using Azasite Drops:


Some medical conditions may interact with Azasite Drops. 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 an allergic reaction (eg, rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue) to a macrolide antibiotic (eg, erythromycin, azithromycin)

Some MEDICINES MAY INTERACT with Azasite Drops. Because little, if any, of Azasite Drops are absorbed into the blood, the risk of it interacting with another medicine is low.


Ask your health care provider if Azasite Drops 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 Azasite Drops:


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


  • Azasite Drops are for use in the eye only. Do not swallow it.

  • Wash your hands immediately before you use Azasite Drops.

  • Turn the bottle upside down and shake once before each use. Remove the cap while the bottle is still upside down.

  • To use Azasite Drops, tilt your head back. Using your index finger, pull the lower eyelid away from the eye to form a pouch. Gently squeeze the bottle to drop the medicine into the pouch, then gently close your eyes. Immediately use your finger to apply pressure to the inside corner of the eye for 1 to 2 minutes. Do not blink. Remove excess medicine around your eye with a clean, dry tissue, being careful not to touch your eye. Wash your hands to remove any medicine that may be on them.

  • To prevent germs from contaminating your medicine, do not touch the applicator tip to any surface, including the eye. Keep the container tightly closed.

  • Do not wear contact lenses while you are using Azasite Drops. Take care of your contact lenses as directed by the manufacturer. Check with your doctor before you use them.

  • To clear up your infection completely, use Azasite Drops for the full course of treatment. Keep using it even if you feel better in a few days.

  • If you miss a dose of Azasite Drops, use 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 use 2 doses at once.

Ask your health care provider any questions you may have about how to use Azasite Drops.



Important safety information:


  • Infrequently, Azasite Drops may cause blurred vision. Use Azasite Drops with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

  • Azasite Drops only works against bacteria; it does not treat viral infections.

  • Be sure to use Azasite Drops 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 Azasite Drops 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.

  • Azasite Drops should be used with extreme caution in CHILDREN younger than 1 year; 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 Azasite Drops while you are pregnant. It is not known if Azasite Drops are found in breast milk after topical use. If you are or will be breast-feeding while you use Azasite Drops, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Azasite Drops:


All medicines may cause side effects, but many people have no, or minor, side effects. No COMMON side effects have been reported with Azasite Drops. 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; unusual hoarseness); discharge from the eye; eye pain; red, swollen, blistered, or peeling skin; severe or persistent burning, stinging, or irritation of the eye; swelling around the eyes; 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: Azasite 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 Azasite Drops:

Store unopened bottles of Azasite Drops in the refrigerator, between 36 and 46 degrees F (2 and 8 degrees C). Once the bottle is opened, it may be stored in the refrigerator or at room temperature below 77 degrees F (25 degrees C). Do not freeze. Store away from heat, moisture, and light. Do not store in the bathroom. Throw away any unused medicine after the bottle has been open for 14 days. Keep Azasite Drops out of the reach of children and away from pets.


General information:


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

  • Azasite Drops 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 Azasite Drops. 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 Azasite resources


  • Azasite Side Effects (in more detail)
  • Azasite Use in Pregnancy & Breastfeeding
  • Azasite Support Group
  • 1 Review for Azasite - Add your own review/rating


Compare Azasite with other medications


  • Conjunctivitis, Bacterial
  • Neonatal Conjunctivitis

Wednesday, 21 September 2016

ketorolac Oral, Intravenous, Injection, Intramuscular



kee-toe-ROLE-ak


Oral route(Tablet)

For short term use only (up to 5 days in adults). Not for use in pediatric patients and not indicated for minor or chronic pain. Contraindicated in patients with peptic ulcer disease, recent GI bleeding or perforation, peri-operative pain in the setting of coronary artery bypass graft (CABG) surgery, advanced renal impairment, risk of renal failure due to volume depletion, cerebrovascular bleeding, hemorrhagic diathesis, incomplete homeostasis, high-risk of bleeding, prophylactic analgesic before major surgery, labor and delivery use, nursing mothers, and concomitant aspirin or NSAID use. Use caution with elderly patients due to high risk of GI adverse events and in patients with cardiovascular disease or risk factors. Adjust dosages for elderly patients, patients under 50 kg, and patients with moderately elevated serum creatinine .


Injection route(Solution)

For short term use only (up to 5 days in adults). Not for use in pediatric patients and not indicated for minor or chronic pain. Contraindicated in patients with peptic ulcer disease, recent GI bleeding or perforation, peri-operative pain in the setting of coronary artery bypass graft (CABG) surgery, advanced renal impairment, risk of renal failure due to volume depletion, cerebrovascular bleeding, hemorrhagic diathesis, incomplete homeostasis, high-risk of bleeding, prophylactic analgesic before major surgery, previously demonstrated hypersensitivity reactions, intrathecal or epidural administration, labor and delivery use, nursing mothers, and concomitant aspirin or NSAID use. Use caution with elderly patients due to high risk of GI adverse events and in patients with cardiovascular disease or risk factors. Adjust dosages for elderly patients, patients under 50 kg, and patients with moderately elevated serum creatinine .



Commonly used brand name(s)

In the U.S.


  • Toradol

  • Toradol IV/IM

Available Dosage Forms:


  • Tablet

  • Solution

  • Injectable

Therapeutic Class: Analgesic


Pharmacologic Class: NSAID


Chemical Class: Acetic Acid (class)


Uses For ketorolac


Ketorolac is used to relieve moderately severe pain, usually pain that occurs after an operation or other painful procedure. It belongs to the group of medicines called nonsteroidal anti-inflammatory drugs (NSAIDs). Ketorolac is not a narcotic and is not habit-forming. It will not cause physical or mental dependence, as narcotics can. However, ketorolac is sometimes used together with a narcotic to provide better pain relief than either medicine used alone.


Ketorolac has side effects that can be very dangerous. The risk of having a serious side effect increases with the dose of ketorolac and with the length of treatment. Therefore, ketorolac should not be used for more than 5 days. Before using ketorolac, you should discuss with your doctor the good that ketorolac can do as well as the risks of using it.


Ketorolac is available only with your doctor's prescription.


Once a medicine has been approved for marketing for a certain use, experience may show that it is also useful for other medical problems. Although these uses are not included in product labeling, ketorolac is used in certain patients with the following medical conditions:


  • Pain after surgery in children

Before Using ketorolac


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 ketorolac, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to ketorolac 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


Studies on ketorolac have been done only in adult patients, and there is no specific information comparing use of ketorolac in children up to 16 years of age with use in other age groups.


Geriatric


Stomach or intestinal problems, swelling of the face, feet, or lower legs, or sudden decrease in the amount of urine may be especially likely to occur in elderly patients, who are usually more sensitive than younger adults to the effects of ketorolac. Also, elderly people are more likely than younger adults to get very sick if the medicine causes stomach problems. Studies in older adults have shown that ketorolac stays in the body longer than it does in younger people. Your doctor will consider this when deciding on how much ketorolac should be given for each dose and how often it should be given.


Pregnancy














Pregnancy CategoryExplanation
1st TrimesterCAnimal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women.
2nd TrimesterCAnimal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women.
3rd TrimesterDStudies 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


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


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking ketorolac, 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 ketorolac 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.


  • Aceclofenac

  • Acemetacin

  • Alclofenac

  • Apazone

  • Aspirin

  • Benoxaprofen

  • Bufexamac

  • Carprofen

  • Clometacin

  • Clonixin

  • Dexketoprofen

  • Diclofenac

  • Diflunisal

  • Dipyrone

  • Droxicam

  • Etodolac

  • Etofenamate

  • Felbinac

  • Fenbufen

  • Fenoprofen

  • Fentiazac

  • Floctafenine

  • Flufenamic Acid

  • Flurbiprofen

  • Ibuprofen

  • Indomethacin

  • Indoprofen

  • Isoxicam

  • Ketoprofen

  • Lornoxicam

  • Meclofenamate

  • Mefenamic Acid

  • Meloxicam

  • Nabumetone

  • Naproxen

  • Niflumic Acid

  • Nimesulide

  • Oxaprozin

  • Oxyphenbutazone

  • Pentoxifylline

  • Phenylbutazone

  • Pirazolac

  • Piroxicam

  • Pirprofen

  • Probenecid

  • Propyphenazone

  • Proquazone

  • Sulindac

  • Suprofen

  • Tenidap

  • Tenoxicam

  • Tiaprofenic Acid

  • Tolmetin

  • Zomepirac

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


  • Abciximab

  • Ardeparin

  • Argatroban

  • Beclamide

  • Beta Glucan

  • Bivalirudin

  • Caramiphen

  • Carbamazepine

  • Certoparin

  • Chlormethiazole

  • Cilostazol

  • Citalopram

  • Clopidogrel

  • Clovoxamine

  • Dabigatran Etexilate

  • Dalteparin

  • Danaparoid

  • Desirudin

  • Diazepam

  • Dipyridamole

  • Enoxaparin

  • Escitalopram

  • Ethotoin

  • Felbamate

  • Femoxetine

  • Flesinoxan

  • Fluoxetine

  • Fluvoxamine

  • Fondaparinux

  • Fosphenytoin

  • Gabapentin

  • Ginkgo

  • Heparin

  • Lacosamide

  • Lepirudin

  • Levetiracetam

  • Mephenytoin

  • Mephobarbital

  • Methotrexate

  • Nadroparin

  • Nefazodone

  • Oxcarbazepine

  • Paraldehyde

  • Paramethadione

  • Parnaparin

  • Paroxetine

  • Pemetrexed

  • Phenacemide

  • Phenobarbital

  • Phenytoin

  • Piracetam

  • Pregabalin

  • Protein C

  • Reviparin

  • Rivaroxaban

  • Rufinamide

  • Sertraline

  • Sibutramine

  • Stiripentol

  • Tacrolimus

  • Tiagabine

  • Ticlopidine

  • Tinzaparin

  • Tirofiban

  • Topiramate

  • Trimethadione

  • Valproic Acid

  • Vigabatrin

  • Vilazodone

  • Zimeldine

  • Zonisamide

Using ketorolac 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.


  • Acebutolol

  • Acetohexamide

  • Alacepril

  • Alprenolol

  • Amiloride

  • Arotinolol

  • Atenolol

  • Azilsartan Medoxomil

  • Azosemide

  • Befunolol

  • Bemetizide

  • Benazepril

  • Bendroflumethiazide

  • Benzthiazide

  • Betaxolol

  • Bevantolol

  • Bisoprolol

  • Bopindolol

  • Bucindolol

  • Bumetanide

  • Bupranolol

  • Buthiazide

  • Candesartan Cilexetil

  • Canrenoate

  • Captopril

  • Carteolol

  • Carvedilol

  • Celiprolol

  • Chlorothiazide

  • Chlorpropamide

  • Chlorthalidone

  • Cilazapril

  • Clopamide

  • Cyclopenthiazide

  • Cyclosporine

  • Delapril

  • Desvenlafaxine

  • Dilevalol

  • Duloxetine

  • Enalaprilat

  • Enalapril Maleate

  • Eprosartan

  • Esmolol

  • Ethacrynic Acid

  • Fosinopril

  • Furosemide

  • Gliclazide

  • Glimepiride

  • Glipizide

  • Gliquidone

  • Glyburide

  • Hydrochlorothiazide

  • Hydroflumethiazide

  • Imidapril

  • Indapamide

  • Irbesartan

  • Labetalol

  • Landiolol

  • Levobetaxolol

  • Levobunolol

  • Lisinopril

  • Lithium

  • Losartan

  • Mepindolol

  • Methyclothiazide

  • Metipranolol

  • Metolazone

  • Metoprolol

  • Milnacipran

  • Moexipril

  • Nadolol

  • Nebivolol

  • Nipradilol

  • Olmesartan Medoxomil

  • Oxprenolol

  • Penbutolol

  • Pentopril

  • Perindopril

  • Pindolol

  • Piretanide

  • Polythiazide

  • Propranolol

  • Quinapril

  • Ramipril

  • Sotalol

  • Spirapril

  • Spironolactone

  • Talinolol

  • Tasosartan

  • Telmisartan

  • Temocapril

  • Tertatolol

  • Timolol

  • Tolazamide

  • Tolbutamide

  • Torsemide

  • Trandolapril

  • Triamterene

  • Trichlormethiazide

  • Valsartan

  • Venlafaxine

  • Xipamide

  • Zofenopril

Interactions with Food/Tobacco/Alcohol


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


Other Medical Problems


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


  • Alcohol abuse or

  • Diabetes mellitus (sugar diabetes) or

  • Edema (swelling of face, fingers, feet or lower legs caused by too much fluid in the body) or

  • Kidney disease or

  • Liver disease (severe) or

  • Systemic lupus erythematosus (SLE)—The chance of serious side effects may be increased

  • Asthma or

  • Heart disease or

  • High blood pressure—Ketorolac may make your condition worse.

  • Bleeding in the brain (history of) or

  • Hemophilia or other bleeding problems—Ketorolac may increase the chance of serious bleeding

  • Bleeding from the stomach or intestines (history of) or

  • Colitis, stomach ulcer, or other stomach or intestinal problems (or history of)—Ketorolac may make stomach or intestinal problems worse. Also, bleeding from the stomach or intestines is more likely to occur during ketorolac treatment in people with these conditions

Proper Use of ketorolac


For patients taking ketorolac tablets:


  • To lessen stomach upset, ketorolac tablets should be taken with food (a meal or a snack) or with an antacid.

  • Take ketorolac with a full glass of water. Also, do not lie down for about 15 to 30 minutes after taking it. This helps to prevent irritation that may lead to trouble in swallowing.

For patients using ketorolac injection:


  • Medicines given by injection are sometimes used at home. If you will be using ketorolac at home, your health care professional will teach you how the injections are to be given. You will also have a chance to practice giving injections. Be certain that you understand exactly how the medicine is to be injected.

For safe and effective use of ketorolac, do not use more of it, do not use it more often, and do not use it for more than 5 days. Using too much of ketorolac increases the chance of unwanted effects, especially in elderly patients.


Ketorolac should be used only when it is ordered by your doctor for treating certain kinds of pain. Because of the risk of serious side effects, do not save any leftover ketorolac for use in the future, and do not share it with other people.


Dosing


The dose of ketorolac 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 ketorolac. 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 form (tablets):
    • For pain:
      • Adults (patients 16 years of age and older)—One 10-milligram (mg) tablet four times a day, four to six hours apart. Some people may be directed to take two tablets for the first dose only.

      • Children up to 16 years of age—Use and dose must be determined by your doctor.



  • For injection dosage form:
    • For pain:
      • Adults (patients 16 years of age and older)—15 or 30 mg, injected into a muscle or a vein four times a day, at least 6 hours apart. This amount of medicine may be contained in 1 mL or in one-half (0.5) mL of the injection, depending on the strength. Some people who do not need more than one injection may receive one dose of 60 mg, injected into a muscle.

      • Children up to 16 years of age—Use and dose must be determined by your doctor.



Missed Dose


If you miss a dose of ketorolac, 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. Do not refrigerate. Keep from freezing.


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Precautions While Using ketorolac


Taking certain other medicines together with ketorolac may increase the chance of unwanted effects. The risk will depend on how much of each medicine you take every day, and on how long you take the medicines together. Therefore, do not take acetaminophen (e.g., Tylenol) together with ketorolac for more than a few days, unless otherwise directed by your medical doctor or dentist. Also, do not take any of the following medicines together with ketorolac, unless your medical doctor or dentist has directed you to do so and is following your progress:


  • Aspirin or other salicylates

  • Diclofenac (e.g., Voltaren®)

  • Diflunisal (e.g., Dolobid®)

  • Etodolac (e.g., Lodine®)

  • Fenoprofen (e.g., Nalfon®)

  • Floctafenine (e.g., Idarac®)

  • Flurbiprofen (e.g., Ansaid®)

  • Ibuprofen (e.g., Motrin®)

  • Indomethacin (e.g., Indocin®)

  • Ketoprofen (e.g., Orudis®)

  • 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®)

  • Zomepirac (e.g., Zomax®)

Ketorolac may cause some people to become dizzy or drowsy. If either of these side effects occurs, do not drive, use machines, or do anything else that could be dangerous if you are not alert.


Serious side effects can occur during treatment with ketorolac. Sometimes serious side effects can occur without any warning. However, possible warning signs often occur, including swelling of the face, fingers, feet, and/or lower legs; severe stomach pain, black, tarry stools, and/or vomiting of blood or material that looks like coffee grounds; unusual weight gain; and/or skin rash. Also, signs of serious heart problems could occur such as chest pain, tightness in chest, fast or irregular heartbeat, or unusual flushing or warmth of skin. Stop taking ketorolac and check with your doctor immediately if you notice any of these warning signs.


ketorolac Side Effects


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


Check with your doctor immediately if any of the following side effects occur:


More common
  • Swelling of face, fingers, lower legs, ankles, and/or feet

  • weight gain (unusual)

Less common
  • Bruising (not at place of injection)

  • high blood pressure

  • skin rash or itching

  • small, red spots on skin

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

Rare
  • Abdominal or stomach pain, cramping, or burning that is severe

  • bleeding from the rectum or bloody or black, tarry stools

  • bloody or cloudy urine

  • blue lips and fingernails

  • blurred vision of other vision change

  • burning, red, tender, thick, scaly, or peeling skin

  • chest pain

  • convulsions

  • cough or hoarseness

  • dark urine

  • decrease in amount of urine that is sudden

  • fainting

  • fast, irregular, noisy, or troubled breathing

  • fever with severe headache, drowsiness, confusion, and stiff neck or back

  • fever with or without chills or sore throat

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

  • hearing loss

  • hives

  • increase in amount of urine or urinating often

  • light-colored stools

  • loss of appetite

  • low blood pressure

  • mood changes or unusual behavior

  • muscle cramps or pain

  • nausea, heartburn, or indigestion that is severe and continues

  • nosebleeds

  • pain in lower back and/or side

  • pain, tenderness, or swelling in the upper stomach area

  • painful or difficult urination

  • pale skin

  • puffiness or swelling of the eyelids or eyes

  • ringing or buzzing in ears

  • runny nose

  • severe restlessness

  • shortness of breath

  • swollen or painful glands

  • swollen tongue

  • thirst that continues

  • tightness in the chest with or without wheezing

  • unusual tiredness or weakness

  • vomiting of blood or material that looks like coffee grounds

  • yellow eyes or skin

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 pain (mild or moderate)

  • bruising at place of injection

  • diarrhea

  • dizziness

  • drowsiness

  • headache

  • indigestion

  • nausea

Less common or rare
  • Bloating or gas

  • burning or pain at place of injection

  • constipation

  • feeling of fullness in abdominal or stomach area

  • increased sweating

  • vomiting

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.



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More ketorolac Oral, Intravenous, Injection, Intramuscular resources


  • Ketorolac Oral, Intravenous, Injection, Intramuscular Use in Pregnancy & Breastfeeding
  • Drug Images
  • Ketorolac Oral, Intravenous, Injection, Intramuscular Drug Interactions
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  • Pain
  • Postoperative Pain

Ketoconazole Shampoo




Dosage Form: shampoo
Ketoconazole Shampoo, 2%

For topical application only.

Rx only



DESCRIPTION


Ketoconazole Shampoo, 2%, is a red-orange liquid for topical application, containing the broad spectrum synthetic antifungal agent ketoconazole, USP in a concentration of 2% in an aqueous suspension. It also contains: sodium laureth sulfate, disodium laureth sulfosuccinate, cocamide diethanolamide, hydrochloric acid, NF, PEG-120 methyl glucose dioleate, imidurea, NF, sodium chloride, USP, sodium hydroxide, NF, fragrance, FD&C red No. 40, and purified water, USP.


Ketoconazole is cis - 1 - acetyl - 4 - [4 - [[2 - (2,4 - dichlorophenyl) - 2 - (1H - imidazol - 1 - ylmethyl) - 1,3 - dioxolan - 4 - yl]methoxy]phenyl]piperazine and has the following structural formula:




CLINICAL PHARMACOLOGY


Tinea (pityriasis) versicolor is a non-contagious infection of the skin caused by Pityrosporum orbiculare (Malassezia furfur). This commensal organism is part of the normal skin flora. In susceptible individuals the condition is often recurrent and may give rise to hyperpigmented or hypopigmented patches on the trunk which may extend to the neck, arms and upper thighs. Treatment of the infection may not immediately result in restoration of pigment to the affected sites. Normalization of pigment following successful therapy is variable and may take months, depending on individual skin type and incidental skin exposure. The rate of recurrence of infection is variable.


Ketoconazole was not detected in plasma in 39 patients who shampooed 4-10 times per week for 6 months, or in 33 patients who shampooed 2-3 times per week for 3-26 months (mean: 16 months).


An exaggerated use washing test on the sensitive antecubital skin of 10 subjects twice daily for five consecutive days showed that the irritancy potential of Ketoconazole Shampoo, 2%, was significantly less than that of 2.5% selenium sulfide shampoo.


A human sensitization test, a phototoxicity study, and a photoallergy study conducted in 38 male and 22 female volunteers showed no contact sensitization of the delayed hypersensitivity type, no phototoxicity and no photoallergenic potential due to Ketoconazole Shampoo, 2%.


Mode of Action: Interpretations of in vivo studies suggest that ketoconazole impairs the synthesis of ergosterol, which is a vital component of fungal cell membranes. It is postulated, but not proven, that the therapeutic effect of ketoconazole in tinea (pityriasis) versicolor is due to the reduction of Pityrosporum orbiculare (Malassezia furfur) and that the therapeutic effect in dandruff is due to the reduction of Pityrosporum ovale. Support for the therapeutic effect in tinea versicolor comes from a three-arm, parallel, double-blind, placebo controlled study in patients who had moderately severe tinea (pityriasis) versicolor. Successful response rates in the primary efficacy population for each of both three-day and single-day regimens of Ketoconazole Shampoo, 2%, were statistically significantly greater (73% and 69%, respectively) than a placebo regimen (5%). There had been mycological confirmation of fungal disease in all cases at baseline. Mycological clearing rates were 84% and 78%, respectively, for the three-day and one-day regimens of the 2% shampoo and 11% in the placebo regimen. While the differences in the rates of successful response between either of the two active treatments and placebo were statistically significant, the difference between the two active regimens was not.


Microbiology: Ketoconazole is a broad spectrum synthetic antifungal agent which inhibits the growth of the following common dermatophytes and yeasts by altering the permeability of the cell membrane: dermatophytes: Trichophyton rubrum, T. mentagrophytes, T. tonsurans, Microsporum canis, M. audouini, M. gypseum and Epidermophyton floccosum; yeasts: Candida albicans, C. tropicalis, Pityrosporum ovale (Malassezia ovale) and Pityrosporum orbiculare (M. furfur). Development of resistance by these microorganisms to ketoconazole has not been reported.



INDICATIONS AND USAGE


Ketoconazole Shampoo, 2%, is indicated for the treatment of tinea (pityriasis) versicolor caused by or presumed to be caused by Pityrosporum orbiculare (also known as Malassezia furfur or M. orbiculare).


Note: Tinea (pityriasis) versicolor may give rise to hyperpigmented or hypopigmented patches on the trunk which may extend to the neck, arms and upper thighs. Treatment of the infection may not immediately result in normalization of pigment to the affected sites. Normalization of pigment following successful therapy is variable and may take months, depending on individual skin type and incidental sun exposure. Although tinea versicolor is not contagious, it may recur because the organism that causes the disease is part of the normal skin flora.



CONTRAINDICATIONS


Ketoconazole Shampoo, 2%, is contraindicated in persons who have known hypersensitivity to the active ingredient or excipients of this formulation.



PRECAUTIONS


Severe hypersensitivity reactions, including anaphylaxis, have been reported during post-marketing use of Ketoconazole Shampoo, 2%.  If a reaction suggesting sensitivity or chemical irritation should occur, use of the medication should be discontinued.



Information for Patients


Patients should be advised of the following:


  • Ketoconazole Shampoo, 2% may be irritating to mucous membranes of the eyes and contact with this area should be avoided.

  • The following have been reported with the use of Ketoconazole Shampoo, 2%: hair discoloration and abnormal hair texture, removal of the curl from permanently waved hair, itching, skin burning sensation and contact dermatitis, hypersensitivity, alopecia, rash, urticaria, skin irritation, dry skin, and application site reactions.

  • Patients who develop allergic reactions, such as generalized rash, skin reactions, severe swelling, or shortness of breath should discontinue Ketoconazole Shampoo, 2% and contact their physician immediately.


Carcinogenesis, Mutagenesis, Impairment of Fertility


Long-term studies to assess the carcinogenic potential of Ketoconazole Shampoo, 2% have not been conducted. A long-term feeding study of ketoconazole in Swiss Albino mice and in Wistar rats showed no evidence of oncogenic activity.  The dominant lethal mutation test in male and female mice revealed that single oral doses of ketoconazole as high as 80 mg/kg were not genotoxic. The Ames Salmonella microsomal activator assay was also negative.



Pregnancy


Teratogenic Effects

Pregnancy Category C: There are no adequate and well-controlled studies in pregnant women.  Ketoconazole should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. In humans, ketoconazole is not detected in plasma after chronic shampooing on the scalp.


Ketoconazole has been shown to be teratogenic (syndactylia and oligodactylia) in the rat when given orally in the diet at 80 mg/kg/day (a dose 10 times the maximum recommended human oral dose). However, these effects may be related to maternal toxicity, which was seen at this and higher dose levels.



Nursing Mothers


There are no adequate and well-controlled studies in nursing women.  Ketoconazole is not detected in plasma after chronic shampooing on the scalp. Caution should be exercised when Ketoconazole Shampoo, 2%, is administered to a nursing woman.



Pediatric Use


Safety and effectiveness in children have not been established.



ADVERSE REACTIONS


In 11 double-blind trials in 264 patients using Ketoconazole Shampoo, 2%, for the treatment of dandruff or seborrheic dermatitis, an increase in normal hair loss and irritation occurred in less than 1% of patients. In three open-label safety trials in which 41 patients shampooed 4-10 times weekly for six months, the following adverse experiences each occurred once: abnormal hair texture, scalp pustules, mild dryness of the skin, and itching. As with other shampoos, oiliness and dryness of hair and scalp have been reported. In a double-blind, placebo-controlled trial in which patients with tinea versicolor were treated with either a single application of Ketoconazole Shampoo, 2%, (n=106), a daily application for three consecutive days (n=107), or placebo (n=105), drug-related adverse events occurred in 5 (5%), 7 (7%) and 4 (4%) of patients, respectively. The only events that occurred in more than one patient in any one of the three treatment groups were pruritus, application site reaction, and dry skin; none of these events occurred in more than 3% of the patients in any one of the three groups.


In worldwide experience with Ketoconazole Shampoo, 2% there have been reports of hair discoloration and abnormal hair texture, itching, skin burning sensation, contact dermatitis, hypersensitivity, alopecia, rash, urticaria, skin irritation, dry skin, and application site reactions. Because these reactions are reported voluntarily from a population of uncertain size, it is not possible to reliably estimate their frequency.



OVERDOSAGE


Ketoconazole Shampoo, 2%, is intended for external use only. In the event of accidental ingestion, supportive measures should be employed. Induced emesis and gastric lavage should usually be avoided.



DOSAGE AND ADMINISTRATION


Apply the shampoo to the damp skin of the affected area and a wide margin surrounding this area. Lather, leave in place for 5 minutes, and then rinse off with water.


One application of the shampoo should be sufficient.



HOW SUPPLIED


Ketoconazole Shampoo, 2%, is a red-orange liquid supplied in a 4-fluid ounce nonbreakable plastic bottle (NDC 0781-7090-04).


Storage conditions:  Store at a temperature not above 25°C (77°F). Protect from light.


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


Manufactured by

TOLMAR Inc., Fort Collins, CO 80526 for

Sandoz Inc., Princeton, NJ 08540


04456 Rev. 5 05/11



PACKAGE LABEL.PRINCIPAL DISPLAY PANEL











KETOCONAZOLE 
ketoconazole  shampoo, suspension










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)0781-7090
Route of AdministrationTOPICALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
KETOCONAZOLE (KETOCONAZOLE)KETOCONAZOLE20.5 mg  in 1 mL
























Inactive Ingredients
Ingredient NameStrength
SODIUM LAURETH SULFATE 
DISODIUM LAURETH SULFOSUCCINATE 
HYDROCHLORIC ACID 
IMIDUREA 
SODIUM CHLORIDE 
SODIUM HYDROXIDE 
COCO DIETHANOLAMIDE 
PEG-120 METHYL GLUCOSE DIOLEATE 
WATER 
FD&C RED NO. 40 


















Product Characteristics
ColorRED (orange)Score    
ShapeSize
FlavorImprint Code
Contains      










Packaging
#NDCPackage DescriptionMultilevel Packaging
10781-7090-04118.28 mL In 1 BOTTLE, PLASTICNone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07694211/04/2005


Labeler - Sandoz Inc. (110342024)









Establishment
NameAddressID/FEIOperations
TOLMAR Inc.791156578MANUFACTURE, ANALYSIS
Revised: 06/2011Sandoz Inc.

More Ketoconazole Shampoo resources


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  • 10 Reviews for Ketoconazole - Add your own review/rating


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  • Cutaneous Candidiasis
  • Dandruff
  • Seborrheic Dermatitis
  • Tinea Corporis
  • Tinea Cruris
  • Tinea Pedis
  • Tinea Versicolor

ketotifen


kee-toe-TYE-fen


Available Dosage Forms:


  • Syrup

  • Tablet

Pharmacologic Class: Mast Cell Stabilizer


Chemical Class: Piperidine


Uses For ketotifen

Ketotifen is a type of asthma medication which, when taken every day and used along with other antiasthma medications, may reduce the frequency, severity, and duration of asthma symptoms or attacks in children. It may also lead to a reduction in daily requirements of other antiasthma medications. Ketotifen is not effective for the prevention or treatment of acute asthma attacks. Ketotifen works by inhibiting certain substances in the body that are known to cause inflammation and symptoms of asthma.


ketotifen is available only with your doctor's prescription.


Before Using ketotifen


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 ketotifen, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to ketotifen 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


ketotifen has been tested in children and, in effective doses, has not been shown to cause different side effects or problems than it does in adults.


Geriatric


Many medicines have not been studied specifically in older people. Therefore, it may not be known whether they work exactly the same way they do in younger adults or if they cause different side effects or problems in older people. There is no specific information comparing use of ketotifen in the elderly with use in other age groups.


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. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine.


Interactions with Food/Tobacco/Alcohol


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


Other Medical Problems


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


  • Diabetes mellitus (sugar diabetes)—May alter low-sugar diet (syrup contains carbohydrates)

  • Epilepsy—May increase risk of convulsions (seizures)

Proper Use of ketotifen


Make certain your health care professional knows if you are on any special diet, such as a low-sugar diet. The syrup contains carbohydrates.


Ketotifen is used to help prevent asthma attacks. It will not relieve an asthma attack that has already started.


Ketotifen must be taken continuously in order to be effective.


Continue taking your current asthma medications until instructed otherwise by your doctor.


Ketotifen may be taken with or without food.


Dosing


The dose of ketotifen 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 ketotifen. 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 form (tablets and syrup):
    • For asthma:
      • Adults and children 3 years of age and older—The usual dose is 1 milligram (mg) (1 tablet or 5 milliliters [mL] of syrup) twice daily, once in the morning and once in the evening.

      • Infants and children from 6 months to 3 years of age—Dose is based on body weight and must be determined by the doctor. It is usually 0.25 mL (50 mcg or 0.05 mg) of syrup per kilogram (kg) (110 micrograms [mcg] or 0.110 mg per pound) of body weight twice daily, once in the morning and once in the evening.



Missed Dose


If you miss a dose of ketotifen, 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 ketotifen


It is very important that your doctor check your progress at regular visits. This will allow your doctor to see if the medicine is working properly and to decide if you should continue to take it. If your symptoms worsen, you should check with your doctor.


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


ketotifen may cause some people to become excited, irritable, or nervous or to have trouble in sleeping. These are symptoms of central nervous system stimulation and are especially likely to occur in children.


For patients with diabetes:


  • The syrup form of ketotifen may affect blood sugar levels. If you notice a change in the results of your blood or urine sugar tests or if you have any questions, check with your doctor.

ketotifen Side Effects


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


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


Less common
  • Chills

  • cough

  • diarrhea

  • fever

  • general feeling of discomfort or illness

  • headache

  • joint pain

  • loss of appetite

  • muscle aches and pains

  • nausea

  • runny nose

  • shivering

  • sore throat

  • sweating

  • trouble sleeping

  • unusual tiredness or weakness

  • vomiting

Rare
  • Abdominal or stomach pain

  • blistering, itching, peeling, or redness of skin

  • bloody or cloudy urine

  • clay-colored stools

  • convulsions

  • dark urine

  • difficult, burning, or painful urination

  • dizziness

  • frequent urge to urinate

  • muscle spasm or jerking of all extremities

  • rash

  • sudden loss of consciousness

  • unpleasant breath odor

  • vomiting of blood

  • yellow eyes or skin

Symptoms of overdose

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


  • Blurred vision

  • confusion

  • convulsions

  • disorientation

  • dizziness

  • drowsiness (severe)

  • faintness or lightheadedness when getting up from a lying or sitting position

  • fast, pounding, or irregular heartbeat or pulse

  • hyperexcitability

  • loss of consciousness

  • palpitations

  • sweating

  • unusual tiredness or weakness

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
  • Weight gain

Less common or rare
  • Bloody nose

  • drowsiness

  • dryness of mouth

  • excitation

  • increased appetite

  • irritability

  • nervousness

  • swelling of eyelids

  • unexplained nosebleeds

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.

See also: ketotifen side effects (in more detail)



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 ketotifen resources


  • Ketotifen Side Effects (in more detail)
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  • Conjunctivitis, Allergic

Tuesday, 20 September 2016

Klor-con Powder



Pronunciation: po-TAS-ee-um KLOR-ide
Generic Name: Potassium Chloride
Brand Name: Examples include Gen-K and Klor-con


Klor-con Powder is used for:

Preventing or treating low blood potassium levels when the amount of potassium in the diet is inadequate. Low potassium levels may also be caused by some diseases, severe or prolonged episodes of vomiting or diarrhea, or by certain medicines (eg, diuretics). Symptoms of low potassium levels include weakness, fatigue, or weakening of reflexes.


Klor-con Powder is an electrolyte that is needed for normal functioning of cells, nerve conduction, muscle contraction, kidney function, and acid-base balance.


Do NOT use Klor-con Powder if:


  • you are allergic to any ingredient in Klor-con Powder

  • you have a high blood potassium level

  • you are taking a potassium-sparing diuretic (eg, triamterene)

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



Before using Klor-con Powder:


Some medical conditions may interact with Klor-con Powder. 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 a high acidity of your body fluids (acidosis), adrenal gland problems, diarrhea, or kidney problems

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


  • Aldosterone blockers (eg, spironolactone), angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril), nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, ibuprofen), or potassium-sparing diuretics (eg, triamterene) because the risk of high blood potassium levels may be increased

This may not be a complete list of all interactions that may occur. Ask your health care provider if Klor-con Powder 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 Klor-con Powder:


Use Klor-con Powder as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Klor-con Powder may cause stomach upset. Take Klor-con Powder by mouth with food or after meals.

  • Dissolve Klor-con Powder in at least half a glass (4 oz/120 mL) of water or juice and drink.

  • Do not lie down for 30 minutes after taking Klor-con Powder.

  • If you miss a dose of Klor-con Powder, take it if you remember within 2 hours. If it is more than 2 hours since your missed dose, skip it 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 Klor-con Powder.



Important safety information:


  • Check with your doctor before you use a salt substitute or a product that has potassium in it.

  • Too much or too little potassium can adversely affect your heart. Be sure that your health care provider and pharmacist are aware of any heart medications that you are taking.

  • Lab tests, including blood electrolytes and kidney function, may be performed while you use Klor-con Powder. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • Use Klor-con Powder with caution in the ELDERLY; they may be more sensitive to its effects.

  • Klor-con Powder should be used with extreme caution in CHILDREN; 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 Klor-con Powder while you are pregnant. It is not known if Klor-con Powder is found in breast milk. If you are or will be breast-feeding while you use Klor-con Powder, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Klor-con Powder:


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; stomach discomfort; 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); black, tarry stools; bleeding in the stomach; chest pain; heart problems; irregular heartbeat; numbness or tingling in the hands or feet; stomach pain; vomit that looks like coffee grounds; weak or heavy legs.



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: Klor-con 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 chest pain; fast, slow, or irregular heartbeat; limp muscles; listlessness; muscle weakness or paralysis; slow or difficult breathing.


Proper storage of Klor-con Powder:

Store Klor-con Powder at room temperature, between 59 and 86 degrees F (15 and 30 degrees C), in a tightly closed container. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Klor-con Powder out of the reach of children and away from pets.


General information:


  • If you have any questions about Klor-con Powder, please talk with your doctor, pharmacist, or other health care provider.

  • Klor-con Powder 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 Klor-con Powder. 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 Klor-con resources


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


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  • Hypokalemia
  • Prevention of Hypokalemia

Magnesium Citrate Solution


Pronunciation: mag-NEE-zee-um SEYE-trate
Generic Name: Magnesium Citrate
Brand Name: Examples include Citrate of Magnesia and LiquiPrep


Magnesium Citrate Solution is used for:

Clearing the bowels before tests or for treating constipation.


Magnesium Citrate Solution is a laxative. It works by attracting and retaining water in the intestine, which allows the bowel to evacuate.


Do NOT use Magnesium Citrate Solution if:


  • you are allergic to any ingredient in Magnesium Citrate Solution

  • you are taking aluminum salt (eg, aluminum hydroxide) or quinolones (eg, ciprofloxacin)

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



Before using Magnesium Citrate Solution:


Some medical conditions may interact with Magnesium Citrate Solution. 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 a history of bowel obstruction or kidney conditions, appendicitis, heart failure, or rectal bleeding

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


  • Aluminum salts (eg, aluminum hydroxide) or anticoagulants (eg, warfarin) because the risk of their side effects may be increased by Magnesium Citrate Solution

  • Bisphosphonates (eg, risedronate), digoxin, penicillamine, quinolone antibiotics (eg, ciprofloxacin), or tetracyclines (eg, doxycycline) because their effectiveness may be decreased by Magnesium Citrate Solution

This may not be a complete list of all interactions that may occur. Ask your health care provider if Magnesium Citrate Solution 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 Magnesium Citrate Solution:


Use Magnesium Citrate Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Take Magnesium Citrate Solution on an empty stomach. Take Magnesium Citrate Solution with a full glass of water (8 oz/240 mL).

  • If you also take a bisphosphonate (eg, alendronic acid), digoxin, or a tetracycline (eg, doxycycline), do not take them within 2 to 4 hours of taking Magnesium Citrate Solution. Check with your doctor if you have questions.

  • If you miss a dose of Magnesium Citrate Solution, take it as soon as you remember. Continue to take it as directed by your doctor or on the package label.

Ask your health care provider any questions you may have about how to use Magnesium Citrate Solution.



Important safety information:


  • Do not use Magnesium Citrate Solution if you experience abdominal pain, nausea, vomiting, or rectal bleeding except under the direction of your doctor.

  • If you notice a sudden change in bowel habits that lasts for 2 weeks or more, check with your doctor and do not use any more of Magnesium Citrate Solution.

  • Do NOT take more than the recommended dose or use for longer than 1 week without checking with your doctor.

  • Magnesium Citrate Solution should not be used in CHILDREN younger than 2 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 Magnesium Citrate Solution while you are pregnant. It is not known if Magnesium Citrate Solution is found in breast milk. If you are or will be breast-feeding while you use Magnesium Citrate Solution, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Magnesium Citrate Solution:


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; stomach discomfort.



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); blood in the stool; cramps; dizziness; fainting; irregular heartbeat; severe diarrhea; sweating; weakness.



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: Magnesium Citrate 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 Magnesium Citrate Solution:

Store Magnesium Citrate Solution 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 Magnesium Citrate Solution out of the reach of children and away from pets.


General information:


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

  • Magnesium Citrate Solution 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 Magnesium Citrate Solution. 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 Magnesium Citrate resources


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


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