Does TIOTROPIUM Cause Product quality issue? 3,821 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,821 reports of Product quality issue have been filed in association with TIOTROPIUM (Tiotropium Bromide). This represents 8.2% of all adverse event reports for TIOTROPIUM.
3,821
Reports of Product quality issue with TIOTROPIUM
8.2%
of all TIOTROPIUM reports
13
Deaths
357
Hospitalizations
How Dangerous Is Product quality issue From TIOTROPIUM?
Of the 3,821 reports, 13 (0.3%) resulted in death, 357 (9.3%) required hospitalization, and 11 (0.3%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIOTROPIUM. However, 3,821 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)
Drug ineffective (3,642)
Loss of personal independence in daily activities (3,414)
Pneumonia (3,046)
Chronic obstructive pulmonary disease (2,895)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
METHYLPHENIDATE (1,728)
Which TIOTROPIUM Alternatives Have Lower Product quality issue Risk?
TIOTROPIUM vs TIPIRACIL\TRIFLURIDINE
TIOTROPIUM vs TIPRANAVIR
TIOTROPIUM vs TIRAGOLUMAB
TIOTROPIUM vs TIRBANIBULIN
TIOTROPIUM vs TIROFIBAN