Does TIOTROPIUM Cause Wrong product administered? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Wrong product administered have been filed in association with TIOTROPIUM (Tiotropium Bromide). This represents 0.0% of all adverse event reports for TIOTROPIUM.
17
Reports of Wrong product administered with TIOTROPIUM
0.0%
of all TIOTROPIUM reports
1
Deaths
4
Hospitalizations
How Dangerous Is Wrong product administered From TIOTROPIUM?
Of the 17 reports, 1 (5.9%) resulted in death, 4 (23.5%) required hospitalization.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIOTROPIUM. However, 17 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which TIOTROPIUM Alternatives Have Lower Wrong product administered Risk?
TIOTROPIUM vs TIPIRACIL\TRIFLURIDINE
TIOTROPIUM vs TIPRANAVIR
TIOTROPIUM vs TIRAGOLUMAB
TIOTROPIUM vs TIRBANIBULIN
TIOTROPIUM vs TIROFIBAN