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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does TIOTROPIUM Cause Intentional product use issue? 223 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 223 reports of Intentional product use issue have been filed in association with TIOTROPIUM (Tiotropium Bromide). This represents 0.5% of all adverse event reports for TIOTROPIUM.

223
Reports of Intentional product use issue with TIOTROPIUM
0.5%
of all TIOTROPIUM reports
2
Deaths
24
Hospitalizations

How Dangerous Is Intentional product use issue From TIOTROPIUM?

Of the 223 reports, 2 (0.9%) resulted in death, 24 (10.8%) required hospitalization, and 1 (0.4%) were considered life-threatening.

Is Intentional product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TIOTROPIUM. However, 223 reports have been filed with the FAERS database.

What Other Side Effects Does TIOTROPIUM Cause?

Dyspnoea (10,863) Incorrect route of drug administration (9,079) Asthma (7,944) Wheezing (5,361) Therapeutic product effect incomplete (4,327) Cough (4,202) Product quality issue (3,821) Drug ineffective (3,642) Loss of personal independence in daily activities (3,414) Pneumonia (3,046)

What Other Drugs Cause Intentional product use issue?

INFLIXIMAB (11,028) RITUXIMAB (9,602) INFLIXIMAB-DYYB (7,549) TOCILIZUMAB (5,078) METHOTREXATE (4,087) PREDNISONE (3,961) ABATACEPT (3,693) ADALIMUMAB (3,557) NIVOLUMAB (3,297) LEFLUNOMIDE (3,280)

Which TIOTROPIUM Alternatives Have Lower Intentional product use issue Risk?

TIOTROPIUM vs TIPIRACIL\TRIFLURIDINE TIOTROPIUM vs TIPRANAVIR TIOTROPIUM vs TIRAGOLUMAB TIOTROPIUM vs TIRBANIBULIN TIOTROPIUM vs TIROFIBAN

Related Pages

TIOTROPIUM Full Profile All Intentional product use issue Reports All Drugs Causing Intentional product use issue TIOTROPIUM Demographics