Does TIOTROPIUM Cause Product dose omission issue? 314 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 314 reports of Product dose omission issue have been filed in association with TIOTROPIUM (Tiotropium Bromide). This represents 0.7% of all adverse event reports for TIOTROPIUM.
314
Reports of Product dose omission issue with TIOTROPIUM
0.7%
of all TIOTROPIUM reports
32
Deaths
223
Hospitalizations
How Dangerous Is Product dose omission issue From TIOTROPIUM?
Of the 314 reports, 32 (10.2%) resulted in death, 223 (71.0%) required hospitalization, and 10 (3.2%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIOTROPIUM. However, 314 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 Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which TIOTROPIUM Alternatives Have Lower Product dose omission issue Risk?
TIOTROPIUM vs TIPIRACIL\TRIFLURIDINE
TIOTROPIUM vs TIPRANAVIR
TIOTROPIUM vs TIRAGOLUMAB
TIOTROPIUM vs TIRBANIBULIN
TIOTROPIUM vs TIROFIBAN