Vesicare Side Effects
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Vesicare Safety Reports reported to FDA
Total Vesicare reports: 1181.Vesicare FDA safety alerts: No.
Reported deaths: 21 Reported hospitalizations: 115.
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Reported Vesicare Side Effects: constipation, dry mouth, vision blurred, urinary retention, pollakiuria, fatigue, headache, oedema peripheral, dizziness, dizziness postural, urinary incontinence.
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Showing 1-50 of 1181 Next >
Vesicare Side Effects Report #5256562-8Consumer or non-health professional from UNITED STATES reported VESICARE problem on Nov 10, 2006. Female patient, 66 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: epistaxis. VESICARE dosage: 5 MG, ORAL. Patient recovered.
Vesicare Side Effects Report #5256563-X
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 28, 2006. Male patient was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: dry mouth, oral pain. VESICARE dosage: unknown. Patient recovered.
Vesicare Side Effects Report #5256565-3
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Nov 01, 2006. Female patient was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: dry mouth, dysgeusia. VESICARE dosage: unknown. Patient recovered.
Vesicare Side Effects Report #5256569-0
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 06, 2006. Female patient, 78 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: feeling abnormal. VESICARE dosage: unknown. Patient recovered.
Vesicare Side Effects Report #5256589-6
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Nov 14, 2006. Female patient, 79 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: insomnia, nocturia. VESICARE dosage: 5 MG, ORAL. Patient recovered.
Vesicare Side Effects Report #5256591-4
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 14, 2006. Female patient was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: rash. VESICARE dosage: 5MG, ORAL. Patient recovered.
Vesicare Side Effects Report #5256592-6
Physician from UNITED STATES reported VESICARE problem on Nov 13, 2006. Female patient, 19 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: crying. VESICARE dosage: 5 MG, ORAL. Patient recovered.
Vesicare Side Effects Report #5256594-X
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 19, 2006. Female patient, 39 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: dizziness, fall. VESICARE dosage: 5 MG, UID/QD. Patient recovered.
Vesicare Side Effects Report #5256599-9
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Nov 13, 2006. Female patient, 68 years of age, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: nocturia, sinus congestion. VESICARE dosage: 5 MG, ORAL. Patient recovered.
Vesicare Side Effects Report #5256600-2
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 13, 2006. Female patient, 58 years of age, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: constipation, dry mouth, incorrect dose administered. VESICARE dosage: 15 MG, UID/QD, ORAL. During the same period patient was treated with AVONEX, LEVOTHYROXINE. Patient recovered.
Vesicare Side Effects Report #5256602-6
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Nov 11, 2006. Female patient was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: muscle spasms. VESICARE dosage: 5 MG, UID/QD, ORAL. Patient recovered.
Vesicare Side Effects Report #5256625-7
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 08, 2006. Female patient, 63 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: alopecia, chest pain, muscle spasms. VESICARE dosage: unknown. Patient recovered.
Vesicare Side Effects Report #5256626-9
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Nov 15, 2006. Female patient, 63 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: diarrhoea. VESICARE dosage: 5 MG, UID/QD, ORAL. Patient recovered.
Vesicare Side Effects Report #5256627-0
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 17, 2006. Female patient, 75 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: constipation, headache. VESICARE dosage: 10 MG, ORAL. Patient recovered.
Vesicare Side Effects Report #5256777-9
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Oct 04, 2006. Female patient, 60 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: urinary incontinence. VESICARE dosage: 5 MG, UID/QD, ORAL. During the same period patient was treated with ASPIRIN, VITAMIN E, SIMVASTATIN, NASONEX, PUFFERS, DETROL. Patient recovered.
Vesicare Side Effects Report #5261337-X
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 21, 2007. Female patient, 64 years of age, was diagnosed with incontinence and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: surgery, vaginal infection. VESICARE dosage: 10 MG, ORAL. During the same period patient was treated with TENORMIN, PRANDIN, ALLOPURINOL, LANTUS, LOMOTIL, XANAX, CHOLESTYRAMINE RESIN. Patient was hospitalized. Patient recovered.
Vesicare Side Effects Report #5261338-1
Physician from UNITED STATES reported VESICARE problem on Feb 16, 2007. Female patient, 78 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: encephalitis, muscle twitching. VESICARE dosage: 10 MG, ORAL. During the same period patient was treated with ACE INHIBITOR NOS, TRIMETHOPRIM SULPHATE, NORVASC. Patient recovered.
Vesicare Side Effects Report #5261596-3
VESICARE problem was reported by a Physician from JAPAN on Feb 23, 2007. Male patient, 90 years of age, weighting 99.21 lb, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: cardiac failure, marasmus. VESICARE dosage: 2.5 MG, UID/QD, ORAL. During the same period patient was treated with LASIX. Patient died on 02/01/2007.
Vesicare Side Effects Report #5261598-7
Physician from JAPAN reported VESICARE problem on Feb 22, 2007. Female patient was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: anorexia, asthenia, diabetes mellitus inadequate control, hyperglycaemia. VESICARE dosage: 5 MG, UID/QD, ORAL. Patient recovered.
Vesicare Side Effects Report #5262742-8
VESICARE problem was reported by a Physician from UNITED STATES on Sept 12, 2006. Female patient, 55 years of age, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: constipation. VESICARE dosage: 5 MG, UID/QD. During the same period patient was treated with ZOVIRAX. Patient recovered.
Vesicare Side Effects Report #5262833-1
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Sept 01, 2006. Female patient, 86 years of age, was diagnosed with urinary incontinence and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: dry mouth. VESICARE dosage: 5 MG, UID/QD, ORAL. Patient recovered.
Vesicare Side Effects Report #5262842-2
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 14, 2006. Male patient was diagnosed with pollakiuria and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: constipation, pollakiuria, vision blurred. VESICARE dosage: 5 MG, ORAL. During the same period patient was treated with COUMADIN, FUROSEMIDE, TOPROL, TRAMADOL. Patient recovered.
Vesicare Side Effects Report #5262855-0
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Sept 25, 2006. Female patient, 76 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: vision blurred. VESICARE dosage: 5 MG, ORAL. Patient recovered.
Vesicare Side Effects Report #5262856-2
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 22, 2006. Female patient, 69 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: constipation, dry mouth. VESICARE dosage: unknown. Patient recovered.
Vesicare Side Effects Report #5262906-3
Health Professional from UNITED STATES reported VESICARE problem on Aug 22, 2006. Female patient was diagnosed with urinary incontinence and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: hypersensitivity, rash. VESICARE dosage: unknown. Patient recovered.
Vesicare Side Effects Report #5262914-2
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 29, 2006. Female patient, 72 years of age, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: abdominal distension, oedema peripheral. VESICARE dosage: 5 MG, UID/QD, ORAL. During the same period patient was treated with ACTOS, SYNTHROID, ATENOLOL. Patient recovered.
Vesicare Side Effects Report #5262915-4
Physician from UNITED STATES reported VESICARE problem on Sept 25, 2006. Male patient was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, constipation, haemorrhoids. VESICARE dosage: 5 MG, ORAL. Patient recovered.
Vesicare Side Effects Report #5262925-7
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 24, 2006. Female patient, 84 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: hyperhidrosis, pruritus. VESICARE dosage: 5 MG, ORAL. Patient recovered.
Vesicare Side Effects Report #5262926-9
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Oct 03, 2006. Female patient, 79 years of age, was diagnosed with urinary incontinence and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: onychoclasis. VESICARE dosage: 5 MG, UID/QD, ORAL. During the same period patient was treated with VITAMINS, BONIVA. Patient recovered.
Vesicare Side Effects Report #5262927-0
VESICARE problem was reported by a Physician from UNITED STATES on Sept 08, 2006. Female patient, 40 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: heart rate increased. VESICARE dosage: 5 MG, ORAL. Patient recovered.
Vesicare Side Effects Report #5262929-4
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Sept 19, 2006. Female patient, 38 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: pruritus, pruritus genital. VESICARE dosage: 5 MG, ORAL. Patient recovered.
Vesicare Side Effects Report #5262940-3
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 20, 2006. Female patient, 69 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: dry mouth, dysphonia, pharyngolaryngeal pain. VESICARE dosage: 10 MG. Patient recovered.
Vesicare Side Effects Report #5262950-6
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Oct 12, 2006. Female patient, 82 years of age, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: constipation, dyspepsia, nausea. VESICARE dosage: unknown. During the same period patient was treated with BENEFIBER, PAXIL, FOSAMAX. Patient recovered.
Vesicare Side Effects Report #5262967-1
VESICARE problem was reported by a Health Professional from UNITED STATES on Nov 17, 2006. Female patient, 72 years of age, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: dyspepsia. VESICARE dosage: 5 MG, ORAL. During the same period patient was treated with SYNTHROID, PLAVIX, LISINOPRIL, QUININE SULPHATE. Patient recovered.
Vesicare Side Effects Report #5262979-8
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Nov 17, 2006. Female patient, 72 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: anorexia, back pain, burning sensation, chills, headache, myalgia, vision blurred. VESICARE dosage: 5 MG, UID/QD, ORAL. Patient recovered.
Vesicare Side Effects Report #5262982-8
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 13, 2006. Male patient was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: rash. VESICARE dosage: unknown. Patient recovered.
Vesicare Side Effects Report #5262983-X
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Nov 17, 2006. Female patient, 90 years of age, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: fatigue, nervousness. VESICARE dosage: 10 MG, ORAL. During the same period patient was treated with SYNTHROID, NEXIUM, DARVOCET. Patient recovered.
Vesicare Side Effects Report #5262984-1
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 31, 2006. Female patient was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, heart rate increased. VESICARE dosage: 5 MG. Patient recovered.
Vesicare Side Effects Report #5262985-3
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Nov 17, 2006. Female patient, 71 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, depression, dizziness, fatigue, nausea, psychomotor hyperactivity. VESICARE dosage: 5 MG, ORAL. During the same period patient was treated with ASPIRIN, DETROL. Patient recovered.
Vesicare Side Effects Report #5262986-5
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 25, 2006. Female patient, 75 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: dry mouth. VESICARE dosage: 5 MG, UID/QD, ORAL. During the same period patient was treated with METFORMIN, PACERONE, QUINAPRIL, NORVASC, TOPROL, LOVASTATIN, WARFARIN, RANITIDINE. Patient recovered.
Vesicare Side Effects Report #5262988-9
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Aug 21, 2006. Male patient was diagnosed with urinary incontinence and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: constipation. VESICARE dosage: 5 MG, UID/QD, ORAL. Patient recovered.
Vesicare Side Effects Report #5262989-0
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 27, 2006. Female patient was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: constipation. VESICARE dosage: 5 MG, UID/QD, ORAL. Patient recovered.
Vesicare Side Effects Report #5262991-9
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Nov 15, 2006. Female patient, 87 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: stomach discomfort. VESICARE dosage: 5 MG, UID/QD, ORAL. Patient recovered.
Vesicare Side Effects Report #5262992-0
VESICARE problem was reported by a Health Professional from UNITED STATES on Oct 31, 2006. Female patient, 80 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: urinary tract infection. VESICARE dosage: 5 MG, ORAL. Patient recovered.
Vesicare Side Effects Report #5262994-4
Physician from UNITED STATES reported VESICARE problem on Aug 22, 2006. Female patient, 72 years of age, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: constipation, dizziness postural, dyspepsia, eructation. VESICARE dosage: unknown. During the same period patient was treated with CIPRO, BACTRIM, ENABLEX. Patient recovered.
Vesicare Side Effects Report #5262996-8
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 25, 2006. Female patient was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: oesophageal pain. VESICARE dosage: 10 MG, ORAL. Patient recovered.
Vesicare Side Effects Report #5262997-X
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Sept 12, 2006. Female patient was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: hypersensitivity, migraine with aura. VESICARE dosage: 5 MG, ORAL. Patient recovered.
Vesicare Side Effects Report #5262998-1
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 28, 2006. Female patient, 65 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: pigmentation disorder. VESICARE dosage: 5 MG, ORAL. During the same period patient was treated with SYNTHROID, CLONIDINE. Patient recovered.
Vesicare Side Effects Report #5262999-3
Consumer or non-health professional from UNITED STATES reported VESICARE problem on Aug 29, 2006. Female patient, 85 years of age, was diagnosed with bladder spasm and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: burning sensation, urethral pain. VESICARE dosage: 5 MG. Patient recovered.
Vesicare Side Effects Report #5263000-8
VESICARE problem was reported by a Physician from UNITED STATES on Sept 19, 2006. Female patient, 68 years of age, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: rash maculo-papular. VESICARE dosage: unknown. During the same period patient was treated with ATENOLOL, AMITRIPTYLINE, HYDROXYZINE, NASONEX, PATANOL, ESTRACE, METROLOTION. Patient recovered.
Showing 1-50 of 1181 Next >
Drug Information: Solifenacin
URL of this page: http://www.nlm.nih.gov/medlineplus/druginfo/medmaster/a605019.html
(sol i fen' a cin)Why is this medication prescribed?
Solifenacin is used to treat overactive bladder (a condition in which the bladder muscles contract uncontrollably and cause frequent urination, urgent need to urinate, and inability to control urination).Solifenacin is in a class of medications called anticholinergics. It works by relaxing the bladder muscles to prevent urgent, frequent, or uncontrolled urination.
How should this medicine be used?
Solifenacin comes as a tablet to take by mouth. It is usually taken once a day with or without food. To help you remember to take solifenacin, take it at around the same time every day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take solifenacin exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.
Swallow the tablets whole; do not split, chew, or crush them. Swallow the tablets with water or another liquid.
Your doctor will probably start you on a low dose of solifenacin and increase your dose later in your treatment.
Solifenacin may help to control your symptoms but will not cure your condition. Continue to take solifenacin even if you feel well. Do not stop taking solifenacin without talking to your doctor.
Other uses for this medicine
This medication may be prescribed for other uses; ask your doctor or pharmacist for more information.
What special precautions should I follow?
Before taking solifenacin,
- tell your doctor and pharmacist if you are allergic to solifenacin, any other medications, or corn.
- tell your doctor and pharmacist what prescription and nonprescription medications, vitamins, and nutritional supplements you are taking. Be sure to mention any of the following: amiodarone (Cordarone, Pacerone); antifungals such as fluconazole (Diflucan), itraconazole (Sporanox), and ketoconazole (Nizoral); carbamazepine (Tegretol); cimetidine (Tagamet); cisapride (Propulsid); clarithromycin (Biaxin); cyclosporine (Neoral, Sandimmune); danazol (Danocrine); delavirdine (Rescriptor); dexamethasone (Decadron); diltiazem (Cardizem, Dilacor, Tiazac); disopyramide (Norpace); dofetilide (Tikosyn); erythromycin (E.E.S., E-Mycin, Erythrocin); ethosuximide (Zarontin); fluoxetine (Prozac, Sarafem); fluvoxamine (Luvox); HIV protease inhibitors such as indinavir (Crixivan) and ritonavir (Norvir); isoniazid (INH, Nydrazid);metronidazole (Flagyl); moxifloxacin (Avelox); nefazodone; phenobarbital (Luminal, Solfoton); phenytoin (Dilantin);pimozide (Orap); procainamide (Procanbid, Pronestyl); quinidine (Quinaglute, Quinidex); rifabutin (Mycobutin); rifampin (Rifadin, Rimactane); sotalol (Betapace); sparfloxacin (Zagam); thioridazine (Mellaril); troglitazone (Rezulin); troleandomycin (TAO); verapamil (Calan, Covera, Isoptin, Verelan); and zafirlukast (Accolate). Your doctor may need to change the doses of your medications or monitor you carefully for side effects.
- tell your doctor what herbal products you are taking, especially St. John's wort.
- tell your doctor if you or any of your family members have or have ever had prolonged QT interval (a problem with the way electricity is conducted in the heart that may cause fainting) or unexplained fainting; and if you have or have ever had glaucoma (an eye disease that can cause vision loss); any type of blockage in the bladder or digestive system; difficulty emptying your bladder or a weak urine stream; myasthenia gravis (a disorder of the nervous system that causes muscle weakness); ulcerative colitis (sores in the intestine that cause stomach pain and diarrhea); benign prostatic hypertrophy (BPH, enlargement of the prostate, a male reproductive organ); constipation; or liver or kidney disease.
- tell your doctor if you are pregnant or plan to become pregnant. If you become pregnant while taking solifenacin, call your doctor. Do not take solifenacin while you are breastfeeding.
- if you are having surgery, including dental surgery, tell the doctor or dentist that you are taking solifenacin.
- you should know that solifenacin may cause blurred vision. Do not drive a car or operate machinery until you know how this medication affects you.
- you should know that solifenacin may make it harder for your body to cool down when it gets very hot. Avoid exposure to extreme heat, and call your doctor or get emergency medical treatment if you have fever or other signs of heat stroke such as dizziness, upset stomach, headache, confusion, and fast pulse after you are exposed to heat.
What special dietary instructions should I follow?
Talk to your doctor about drinking grapefruit juice while taking this medicine.
What should I do if I forget a dose?
Skip the missed dose and take your next dose at the regular time the next day. Do not take two doses of solifenacin in the same day.
What side effects can this medication cause?
Solifenacin may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away:
- dry mouth
- constipation
- stomach pain
- upset stomach
- vomiting
- heartburn
- dry eyes
- blurred vision
- extreme tiredness
Some side effects can be serious. The following symptoms are uncommon, but if you experience any of them, call your doctor immediately:
- severe stomach pain
- constipation that lasts longer than 3 days
- painful or frequent urination
- bloody or cloudy urine
- back pain
- swelling of the face, throat, tongue, lips, eyes, hands, feet, ankles, or lower legs
- hoarseness
- difficulty breathing or swallowing
Solifenacin may cause other side effects. Call your doctor if you have any unusual problems while taking this medication.
If you experience a serious side effect, you or your doctor may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online [at http://www.fda.gov/MedWatch/index.html] or by phone [1-800-332-1088].
What storage conditions are needed for this medicine?
Keep this medication in the container it came in, tightly closed, and out of reach of children. Store it at room temperature and away from excess heat and moisture (not in the bathroom). Throw away any medication that is outdated or no longer needed. Talk to your pharmacist about the proper disposal of your medication.
In case of emergency/overdose
In case of overdose, call your local poison control center at 1-800-222-1222. If the victim has collapsed or is not breathing, call local emergency services at 911.
Symptoms of overdose may include:
- flushing
- dry mouth
- dry eyes
- blurred vision
- enlarged pupils (black circle in the middle of the eye)
- confusion
- fever
- fast heartbeat
- shaking hands that you cannot control
- difficulty walking
- hallucinations (seeing things or hearing voices that do not exist)
- coma
- collapse
What other information should I know?
Keep all appointments with your doctor .
Do not let anyone else take your medication. Ask your pharmacist any questions you have about refilling your prescription.
It is important for you to keep a written list of all of the prescription and nonprescription (over-the-counter) medicines you are taking, as well as any products such as vitamins, minerals, or other dietary supplements. You should bring this list with you each time you visit a doctor or if you are admitted to a hospital. It is also important information to carry with you in case of emergencies.
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