Does TIOTROPIUM Cause Device delivery system issue? 74 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 74 reports of Device delivery system issue have been filed in association with TIOTROPIUM (Tiotropium Bromide). This represents 0.2% of all adverse event reports for TIOTROPIUM.
74
Reports of Device delivery system issue with TIOTROPIUM
0.2%
of all TIOTROPIUM reports
0
Deaths
4
Hospitalizations
How Dangerous Is Device delivery system issue From TIOTROPIUM?
Of the 74 reports, 4 (5.4%) required hospitalization, and 1 (1.4%) were considered life-threatening.
Is Device delivery system issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIOTROPIUM. However, 74 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 Device delivery system issue?
ALBUTEROL (9,509)
SOMATROPIN (1,848)
EXENATIDE (1,533)
BUDESONIDE\FORMOTEROL (1,260)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (1,181)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (523)
LEVALBUTEROL (459)
MOMETASONE FUROATE\OLOPATADINE (347)
ABATACEPT (342)
PEGFILGRASTIM (323)
Which TIOTROPIUM Alternatives Have Lower Device delivery system issue Risk?
TIOTROPIUM vs TIPIRACIL\TRIFLURIDINE
TIOTROPIUM vs TIPRANAVIR
TIOTROPIUM vs TIRAGOLUMAB
TIOTROPIUM vs TIRBANIBULIN
TIOTROPIUM vs TIROFIBAN