Does OLODATEROL\TIOTROPIUM Cause Product complaint? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product complaint have been filed in association with OLODATEROL\TIOTROPIUM. This represents 0.1% of all adverse event reports for OLODATEROL\TIOTROPIUM.
6
Reports of Product complaint with OLODATEROL\TIOTROPIUM
0.1%
of all OLODATEROL\TIOTROPIUM reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product complaint From OLODATEROL\TIOTROPIUM?
Of the 6 reports, 1 (16.7%) required hospitalization.
Is Product complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OLODATEROL\TIOTROPIUM. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does OLODATEROL\TIOTROPIUM Cause?
Dyspnoea (1,149)
Wheezing (575)
Asthma (526)
Cough (485)
Drug ineffective (403)
Chronic obstructive pulmonary disease (373)
Therapeutic product effect incomplete (319)
Loss of personal independence in daily activities (307)
Pneumonia (280)
Off label use (265)
What Other Drugs Cause Product complaint?
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417)
ALBUTEROL (2,291)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826)
FLUTICASONE\SALMETEROL (1,601)
MEPOLIZUMAB (1,296)
FLUTICASONE (1,112)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108)
BELIMUMAB (1,079)
SUMATRIPTAN (718)
NICOTINE (700)
Which OLODATEROL\TIOTROPIUM Alternatives Have Lower Product complaint Risk?
OLODATEROL\TIOTROPIUM vs OLOPATADINE
OLODATEROL\TIOTROPIUM vs OLUTASIDENIB
OLODATEROL\TIOTROPIUM vs OMACETAXINE MEPESUCCINATE
OLODATEROL\TIOTROPIUM vs OMADACYCLINE
OLODATEROL\TIOTROPIUM vs OMALIZUMAB