Spiriva Safety Questions, Spiriva Answers
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Spiriva Safety Reports
Total Spiriva reports: 1248.Spiriva FDA safety alerts: 2008 .
Reported deaths: 77 Reported hospitalizations: 267.
Take Spiriva Side Effects Survey or Share Your Spiriva Story.
Reported Spiriva Side Effects: dyspnoea, dry mouth, ageusia, dyspnoea exertional, cough, constipation, dysgeusia, pneumonia, vision blurred, dysphonia, nausea.
Spiriva Usage.
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Spiriva Side Effects Report #5232870-1Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Aug 31, 2006. Female patient was diagnosed with chronic obstructive pulmonary disease, emphysema and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dyspnoea. SPIRIVA dosage: unknown. Patient recovered.
Spiriva Side Effects Report #5232873-7
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 31, 2006. Female patient was diagnosed with chronic obstructive pulmonary disease, emphysema and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: chest discomfort, influenza like illness, musculoskeletal chest pain. SPIRIVA dosage: unknown. During the same period patient was treated with ALBUTEROL, DUO NEB. Patient recovered.
Spiriva Side Effects Report #5232877-4
Physician from UNITED STATES reported SPIRIVA problem on Sept 26, 2006. Male patient, 62 years of age, weighting 120.0 lb, was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dysuria, prostatic disorder, pyrexia, urine flow decreased. SPIRIVA dosage: unknown. During the same period patient was treated with FISH OIL. Patient recovered.
Spiriva Side Effects Report #5232879-8
SPIRIVA problem was reported by a Physician from UNITED STATES on Sept 26, 2006. Female patient, 79 years of age, weighting 115.0 lb, was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: condition aggravated. SPIRIVA dosage: unknown. During the same period patient was treated with QVAR, SEREVENT, SEGRILINE, XANAX, DARVOCET, LISINOPRIL, LEVOTHYROXINE. Patient recovered.
Spiriva Side Effects Report #5232896-8
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Aug 31, 2006. Female patient was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dry mouth, epistaxis, peripheral vascular disorder. SPIRIVA dosage: unknown. Patient recovered.
Spiriva Side Effects Report #5232968-8
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 02, 2006. Female patient, 83 years of age, was diagnosed with asthma, chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: increased upper airway secretion, malaise. SPIRIVA dosage: unknown. Patient recovered.
Spiriva Side Effects Report #5232969-X
Physician from UNITED STATES reported SPIRIVA problem on Sept 29, 2006. Female patient was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: pollakiuria, rash. SPIRIVA dosage: unknown. Patient recovered.
Spiriva Side Effects Report #5232971-8
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 02, 2006. Male patient was diagnosed with pulmonary fibrosis and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: chest discomfort. SPIRIVA dosage: unknown. During the same period patient was treated with ZOCOR, ASPIRIN, MUCINEX. Patient recovered.
Spiriva Side Effects Report #5232975-5
Physician from UNITED STATES reported SPIRIVA problem on Oct 25, 2006. Male patient, 82 years of age, weighting 220.9 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: eye burns, eye pruritus, haematospermia, rash, red blood cells semen. SPIRIVA dosage: unknown. During the same period patient was treated with ALBUTEROL, FLOVENT HFA, ADVAIR DISCUS, PREDNISONE, AUGMENTIN, MONTELUKAST, THEOPHYLLINE. Patient recovered.
Spiriva Side Effects Report #5232979-2
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 18, 2006. Female patient, 65 years of age, weighting 106.0 lb, was diagnosed with chronic obstructive pulmonary disease, emphysema and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, constipation, hypersensitivity, tinnitus. SPIRIVA dosage: unknown. During the same period patient was treated with ALBUTEROL MDI, OXYGEN, CARDIZEM, ELAVIL, DILTIAZEM, AMITRIPTYLINE, COMBIVENT. Patient recovered.
Spiriva Side Effects Report #5232981-0
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Oct 25, 2006. Female patient, 83 years of age, was diagnosed with chronic obstructive pulmonary disease, emphysema and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dyspnoea. SPIRIVA dosage: unknown. During the same period patient was treated with OXYGEN, LOVASTATIN, FUROSEMIDE, ASPIRIN, ALBUTEROL, ISOSORBIDE. Patient recovered.
Spiriva Side Effects Report #5232982-2
SPIRIVA problem was reported by a Physician from UNITED STATES on Oct 05, 2006. Female patient, 80 years of age, was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: visual disturbance. SPIRIVA dosage: unknown. Patient recovered.
Spiriva Side Effects Report #5232994-9
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Sept 26, 2006. Female patient was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dyspnoea, productive cough. SPIRIVA dosage: unknown. Patient recovered.
Spiriva Side Effects Report #5232999-8
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 29, 2006. Female patient, 59 years of age, was diagnosed with asthma, gastrooesophageal reflux disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, eructation, muscle spasms, sinusitis. SPIRIVA dosage: unknown. During the same period patient was treated with PREDNISONE, ADVAIR, ALLEGRA, PREVACID, ALBUTEROL, VITAMIN, CALCIUM. Patient recovered.
Spiriva Side Effects Report #5233001-4
Physician from UNITED STATES reported SPIRIVA problem on Sept 12, 2006. Female patient, 26 years of age, was diagnosed with obstructive airways disorder and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: chest pain, pruritus, rash, rash papular. SPIRIVA dosage: unknown. During the same period patient was treated with ALBUTEROL INHALER. Patient recovered.
Spiriva Side Effects Report #5233003-8
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on July 31, 2006. Male patient was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident. SPIRIVA dosage: unknown. During the same period patient was treated with REPORTED IN NARRATIVE. Patient recovered.
Spiriva Side Effects Report #5233004-X
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Aug 02, 2006. Female patient, 65 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: back pain, chest pain, dry mouth. SPIRIVA dosage: unknown. During the same period patient was treated with BENADRYL, OXYGEN. Patient recovered.
Spiriva Side Effects Report #5233011-7
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 02, 2006. Male patient was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dry mouth, dry skin, dry throat, dysphonia. SPIRIVA dosage: unknown. Patient recovered.
Spiriva Side Effects Report #5233013-0
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Aug 02, 2006. Male patient was diagnosed with dyspnoea and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: chest pain, dyspnoea, pharyngolaryngeal pain. SPIRIVA dosage: unknown. During the same period patient was treated with MUCINEX, AMBIEN. Patient recovered.
Spiriva Side Effects Report #5233025-7
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 27, 2006. Male patient, 76 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: cough, odynophagia, pharyngolaryngeal pain. SPIRIVA dosage: unknown. During the same period patient was treated with OXYGEN, IBUPROFEN, TYLENOL W, ALBUTEROL, IPRATROPIUM BROMIDE. Patient recovered.
Spiriva Side Effects Report #5233057-9
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Sept 27, 2006. Female patient was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: somnolence. SPIRIVA dosage: unknown. Patient recovered.
Spiriva Side Effects Report #5233059-2
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 25, 2006. Male patient was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: skin laceration. SPIRIVA dosage: unknown. During the same period patient was treated with BLOOD THINNER. Patient recovered.
Spiriva Side Effects Report #5233061-0
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Oct 10, 2006. Female patient, 75 years of age, was diagnosed with emphysema and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: asthenia, dysphonia, eyelid disorder. SPIRIVA dosage: unknown. During the same period patient was treated with CHOLESTEROL MEDICINE, OXYGEN, TRICOR, NORVASC, BENICAR, CLONIDINE, PROTONIX. Patient recovered.
Spiriva Side Effects Report #5233063-4
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 20, 2006. Female patient, 71 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: visual acuity reduced. SPIRIVA dosage: unknown. During the same period patient was treated with OXYGEN, VERAPAMIL, FOSINOPRIL, LASIX, COUMADIN, COMBIVENT. Patient recovered.
Spiriva Side Effects Report #5233064-6
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Sept 28, 2006. Female patient, 85 years of age, weighting 108.0 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: constipation, haemorrhoidal haemorrhage. SPIRIVA dosage: unknown. During the same period patient was treated with COUMADIN, FUROSEMIDE, AMARYL, CARTIA, ALTACE, DIGOXIN, POTASSIUM CHLORIDE, RHYTHMOL. Patient recovered.
Spiriva Side Effects Report #5233066-X
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 28, 2006. Female patient, 86 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dyspepsia, glossodynia. SPIRIVA dosage: unknown. During the same period patient was treated with NORVASC, LISINOPRIL, DOXAZOSIN, ALBUTEROL. Patient recovered.
Spiriva Side Effects Report #5233073-7
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Sept 29, 2006. Female patient was diagnosed with chronic obstructive pulmonary disease, hypertension and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dysphagia, intracranial aneurysm, pharyngeal oedema, pyrexia. SPIRIVA dosage: unknown. During the same period patient was treated with COZAAR, VITAMIN D, CARDIZEM, INSULIN, BUMEX, ASPIRIN, ALBUTEROL, LEXAPRO. Patient recovered.
Spiriva Side Effects Report #5233075-0
SPIRIVA problem was reported by a Physician from UNITED STATES on Sept 28, 2006. Female patient was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: lipids abnormal. SPIRIVA dosage: unknown. Patient recovered.
Spiriva Side Effects Report #5233077-4
Physician from UNITED STATES reported SPIRIVA problem on Sept 28, 2006. Female patient was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: joint swelling. SPIRIVA dosage: unknown. Patient recovered.
Spiriva Side Effects Report #5233081-6
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 17, 2006. Female patient, 75 years of age, was diagnosed with bronchiectasis, chronic obstructive pulmonary disease, extranodal marginal zone b-cell lymphoma (malt type) and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: cellulitis, oral candidiasis, tongue geographic. SPIRIVA dosage: 18 MG (18 MG,1 IN 1 D),IH. During the same period patient was treated with RUTUXIN. Patient recovered.
Spiriva Side Effects Report #5233083-X
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Oct 17, 2006. Male patient, 49 years of age, was diagnosed with asthma and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dry mouth, dyspnoea, wheezing. SPIRIVA dosage: unknown. During the same period patient was treated with NORVASC, PEROXITINE, PRAVASTATIN, ISOSORBIDE, ASPIRIN, IBUPROFEN. Patient recovered.
Spiriva Side Effects Report #5233089-0
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 18, 2006. Male patient, 48 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dry mouth, dyspnoea. SPIRIVA dosage: unknown. During the same period patient was treated with FUZEON, ANTIDEPRESSANTS, ADVAIR, CPAP TREATMENTS, ALBUTEROL. Patient recovered.
Spiriva Side Effects Report #5233091-9
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Oct 18, 2006. Male patient, 80 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: erythema, eye pruritus, swelling face. SPIRIVA dosage: unknown. During the same period patient was treated with LASIX, FLOMAX, CALCITRIOL, PLAVIX, ATENOLOL, NORVASC, COMBIVENT, ADVAIR. Patient recovered.
Spiriva Side Effects Report #5233094-4
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 19, 2006. Female patient was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: skin laceration. SPIRIVA dosage: unknown. Patient recovered.
Spiriva Side Effects Report #5233111-1
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Oct 19, 2006. Female patient was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: mouth ulceration. SPIRIVA dosage: unknown. Patient recovered.
Spiriva Side Effects Report #5233112-3
SPIRIVA problem was reported by a Physician from UNITED STATES on Oct 18, 2006. Female patient was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: aphonia. SPIRIVA dosage: unknown. During the same period patient was treated with ALPHA. Patient recovered.
Spiriva Side Effects Report #5233117-2
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Sept 13, 2006. Female patient, 63 years of age, weighting 150.0 lb, was diagnosed with lung infection and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: fungal infection, insomnia, lung infection, malaise, vision blurred. SPIRIVA dosage: unknown. During the same period patient was treated with CHANIX, PREDNISONE, ADVAIR DISCUS, XOPENEX, XANAX, ZYRTEC D. Patient recovered.
Spiriva Side Effects Report #5233119-6
SPIRIVA problem was reported by a Health Professional from UNITED STATES on Aug 25, 2006. Male patient, 51 years of age, weighting 198.0 lb, was diagnosed with asthma and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: chills, influenza like illness, muscle twitching. SPIRIVA dosage: unknown. During the same period patient was treated with GLUCOPHAGE, METFORMIN. Patient recovered.
Spiriva Side Effects Report #5233120-2
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Aug 01, 2006. Male patient, 70 years of age, was diagnosed with emphysema and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dysgeusia. SPIRIVA dosage: unknown. During the same period patient was treated with ADVAIR, LIPITOR, ZETIA. Patient recovered.
Spiriva Side Effects Report #5233121-4
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 31, 2006. Female patient, 60 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dysgeusia, dyspnoea. SPIRIVA dosage: unknown. During the same period patient was treated with ALBUTEROL NEBULIZER, COMBIVENT, UNIPHYL, VOLMAX, XANAX, LORTAB, WARFARIN. Patient recovered.
Spiriva Side Effects Report #5233122-6
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Sept 01, 2006. Male patient was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: constipation, dyspnoea. SPIRIVA dosage: unknown. During the same period patient was treated with ALBUTEROL, ANDRODERM, ASPIRIN. Patient recovered.
Spiriva Side Effects Report #5233128-7
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 18, 2006. Female patient, 62 years of age, was diagnosed with chronic obstructive pulmonary disease, emphysema and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: feeling abnormal. SPIRIVA dosage: unknown. During the same period patient was treated with METHOTREXATE, ACTONEL, ADVAIR, THYROID, FOLIC ACID, CALCIUM. Patient recovered.
Spiriva Side Effects Report #5233131-7
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Aug 01, 2006. Male patient, 79 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dyspepsia, eructation. SPIRIVA dosage: unknown. During the same period patient was treated with ATROVENT, LISINOPRIL, DIGOXIN, FUROSEMIDE, PLAVIX, METOPROLOL TARTRATE, ZOCOR. Patient recovered.
Spiriva Side Effects Report #5233132-9
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 20, 2006. Male patient, 70 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dyspnoea. SPIRIVA dosage: unknown. During the same period patient was treated with PREDNISONE, ALBUTEROL. Patient recovered.
Spiriva Side Effects Report #5233138-X
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Aug 17, 2006. Female patient was diagnosed with chronic obstructive pulmonary disease, emphysema and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: ageusia. SPIRIVA dosage: unknown. During the same period patient was treated with ADVAIR. Patient recovered.
Spiriva Side Effects Report #5233139-1
SPIRIVA problem was reported by a Pharmacist from UNITED STATES on Oct 23, 2006. Female patient was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: asthma. SPIRIVA dosage: unknown. Patient recovered.
Spiriva Side Effects Report #5233140-8
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Oct 21, 2006. Female patient was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: feeling jittery, nausea. SPIRIVA dosage: unknown. During the same period patient was treated with IPRATROPIUM BROMIDE, ZOPINEX. Patient recovered.
Spiriva Side Effects Report #5233146-9
SPIRIVA problem was reported by a Physician from UNITED STATES on Oct 20, 2006. Female patient was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dysgeusia. SPIRIVA dosage: unknown. Patient recovered.
Spiriva Side Effects Report #5233147-0
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Oct 23, 2006. Male patient was diagnosed with emphysema and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: anxiety, psychomotor hyperactivity, total lung capacity decreased. SPIRIVA dosage: unknown. During the same period patient was treated with PREDNISONE, AZMACORT, THEOPHYLLINE, ALBUTEROL INHALER. Patient recovered.
Spiriva Side Effects Report #5233149-4
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 25, 2006. Female patient, 77 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dry eye, eye pruritus, skin disorder, vision blurred. SPIRIVA dosage: unknown. During the same period patient was treated with THYROID. Patient recovered.
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Drug Information: Tiotropium Oral Inhalation
URL of this page: http://www.nlm.nih.gov/medlineplus/druginfo/medmaster/a604018.html
(tee oh tro' pee um)IMPORTANT WARNING:
| [Posted 03/18/2008] Boehringer Ingelheim and FDA notified healthcare professionals that ongoing safety monitoring has identified a possible increased risk of stroke in patients who take tiotropium bromide (Spiriva). This product contains tiotropium bromide and is used to treat bronchospasm associated with chronic obstructive pulmonary disease. Boehringer Ingelheim reported to the FDA that it has conducted an analysis of the safety data from 29 placebo controlled clinical studies (“pooled analysis”). Based on data from these studies, the preliminary estimates of the risk of stroke are 8 patients per 1000 patients treated for one year with tiotropium bromide, and 6 patients per 1000 patients treated for one year with placebo. This means that the estimated excess risk of any type of stroke due to tiotropium bromide is 2 patients for each 1000 patients using tiotropium bromide over a one year period.It is important to interpret these preliminary results with caution. FDA is working with Boehringer Ingelheim to further evaluate the potential association between tiotropium bromide and stroke. FDA has not confirmed these analyses and while pooled analyses can provide early information about potential safety issues, these analyses have inherent limitations and uncertainty that require further investigation using other data sources. Patients should not stop taking Spiriva HandiHaler before talking to their doctor, if they have questions about this new information. This early communication is in keeping with FDA’s commitment to inform the public about its ongoing safety reviews of drugs. For more information visit the FDA website at: http://www.fda.gov/medwatch/safety/2008/safety08.htm#Tiotropium and http://www.fda.gov/cder/drug/early_comm/tiotropium.htm. |
Why is this medication prescribed?
Tiotropium is used to prevent wheezing, shortness of breath, and difficulty breathing in patients with chronic obstructive pulmonary disease (COPD, a group of diseases that affect the lungs and airways) such as chronic bronchitis (swelling of the air passages that lead to the lungs) and emphysema (damage to air sacs in the lungs). Tiotropium is in a class of medications called bronchodilators. It works by relaxing and opening the air passages to the lungs to make breathing easier.
How should this medicine be used?
Pending revision, the material in this section should be considered in light of more recently available information in the MedWatch notification at the beginning of this monograph.
Tiotropium comes as a capsule to use with a specially designed inhaler. You will use the inhaler to breathe in the dry powder contained in the capsules. Tiotropium is usually inhaled once a day in the morning or evening. To help you remember to inhale tiotropium, inhale it 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. Use tiotropium exactly as directed. Do not inhale more or less of it or inhale it more often than prescribed by your doctor.
Do not swallow tiotropium capsules.
Tiotropium will only work if you use the inhaler it comes with to inhale the powder in the capsules. Never try to inhale them using any other inhaler. Never use your tiotropium inhaler to take any other medication.
Do not use tiotropium to treat a sudden attack of wheezing or shortness of breath. Your doctor will probably prescribe a different medication to use when you have great difficulty breathing.
Tiotropium controls COPD but does not cure it. It may take a few weeks before you feel the full benefits of tiotropium. Continue to take tiotropium even if you feel well. Do not stop taking tiotropium without talking to your doctor.
Be careful not to get tiotropium powder in your eyes. If tiotropium powder gets into your eyes, your vision may become blurred and you may be sensitive to light. Call your doctor if this happens.
To use the inhaler, follow these steps:
- Use the diagram in the patient information that came with your medication to help you learn the names of the parts of your inhaler. You should be able to find the dust cap, mouthpiece, base, piercing button, and center chamber.
- Pick up one blister card of tiotropium capsules and tear it along the perforation. You should now have two strips that each contain three capsules.
- Put away one of the strips for later. Use the tab to carefully peel back the foil on the other blister strip until the STOP line. This should fully uncover one capsule. The other two capsules on the strip should still be sealed in their packaging. Plan to use those capsules on the next 2 days.
- Pull upward on the dust cap of your inhaler to open it.
- Open the mouthpiece of the inhaler. Remove the tiotropium capsule from the package and place it in the center chamber of the inhaler.
- Close the mouthpiece firmly until it clicks, but do not close the dust cap.
- Hold the inhaler so that the mouthpiece is on top. Press the green piercing button once, then let it go.
- Breathe out completely without putting any part of the inhaler in or near your mouth.
- Bring the inhaler up to your mouth and close your lips tightly around the mouthpiece.
- Hold your head upright and breathe in slowly and deeply. You should breathe just fast enough to hear the capsule vibrate. Continue to breathe in until your lungs are full.
- Hold your breath for as long as you can comfortably do so. Take the inhaler out of your mouth while you are holding your breath.
- Breathe normally for a short time.
- Repeat steps 8-11 to inhale any medication that may be left in your inhaler.
- Open the mouthpiece and tilt the inhaler to spill out the used capsule. Throw the used capsule away out of the reach of children and pets. You may see a small amount of powder remaining in the capsule. This is normal and does not mean that you did not get your full dose.
- Close the mouthpiece and dust cap and store the inhaler in a safe place.
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?
Pending revision, the material in this section should be considered in light of more recently available information in the MedWatch notification at the beginning of this monograph.
Before using tiotropium,
- tell your doctor and pharmacist if you are allergic to tiotropium, atropine (Atropen, Sal-Tropine, Ocu-Tropine), ipratropium (Atrovent), or any other medications.
- tell your doctor and pharmacist what prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking. Be sure to mention any of the following: amiodarone (Cordarone); antihistamines; atropine (Atropen, Sal-Tropine, Ocu-Tropine); cisapride (Propulsid); disopyramide (Norpace); dofetilide (Tikosyn); erythromycin (E.E.S, E-Mycin, Erythrocin); eye drops; ipratropium (Atrovent); medications for irritable bowel disease, motion sickness, Parkinson's disease, ulcers, or urinary problems; moxifloxacin (Avelox); pimozide (Orap); procainamide (Procanbid, Pronestyl); quinidine (Quinidex); sotalol (Betapace); sparfloxacin (Zagam); and thioridazine (Mellaril). Your doctor may need to change the doses of your medications or monitor you carefully for side effects.
- tell your doctor if you have or have ever had glaucoma (an eye disease that can cause vision loss), urinary problems, irregular heart beat, or prostate (a male reproductive organ) or kidney disease.
- tell your doctor if you are pregnant, plan to become pregnant, or are breast-feeding. If you become pregnant while taking tiotropium, call your doctor.
- if you are having surgery, including dental surgery, tell the doctor or dentist that you are taking tiotropium.
What special dietary instructions should I follow?
Unless your doctor tells you otherwise, continue your normal diet.
What should I do if I forget a dose?
Inhale the missed dose as soon as you remember it. However, if it is almost time for the next dose, skip the missed dose and continue your regular dosing schedule. Do not inhale a double dose to make up for a missed one.
What side effects can this medication cause?
Tiotropium may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away:
- dry mouth
- constipation
- stomach pain
- vomiting
- indigestion
- muscle pain
- nosebleed
- runny nose
- sneezing
- painful white patches in mouth
Some side effects can be serious. The following symptoms are uncommon, but if you experience any of them, call your doctor immediately:
- hives
- skin rash
- itching
- difficulty breathing or swallowing
- swelling of the face, throat, tongue, lips, eyes, hands, feet, ankles, or lower legs
- hoarseness
- chest pain
- sore throat, fever, chills, and other signs of infection
- headaches or other signs of a sinus infection
- painful or difficult urination
- fast heart beat
- eye pain
- blurred vision
- seeing halos around lights or seeing colored images
- red eyes
Tiotropium may cause other side effects. Call your doctor if you have any unusual problems while using 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). Do not open the blister package surrounding a capsule until just before you are ready to use it. If you accidentally open the package of a capsule that you cannot use immediately, throw away that capsule. Never store capsules inside the inhaler. 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:
- dry mouth
- stomach pain
- constipation
- shaking hands that you cannot control
- changes in thinking
- blurred vision
- red eyes
- fast heartbeat
- difficulty urinating
What other information should I know?
Pending revision, the material in this section should be considered in light of more recently available information in the MedWatch notification at the beginning of this monograph.
Keep all appointments with your doctor.
You will receive a new inhaler with each 30 day supply of medication. Normally, you will not need to clean your inhaler during the 30 days you use it. However, if you do need to clean your inhaler, you should open the dust cap and mouthpiece and then press the piercing button to open the base. Then rinse the entire inhaler with warm water but without any soaps or detergents. Tip out excess water and leave the inhaler to air dry for 24 hours with the dust cap, mouthpiece, and base open. Do not wash your inhaler in the dishwasher and do not use it after you wash it until it has been allowed to dry for 24 hours. You may also clean the outside of the mouthpiece with a moist (not wet) tissue.
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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