Does OLODATEROL\TIOTROPIUM Cause Product administration error? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product administration error have been filed in association with OLODATEROL\TIOTROPIUM. This represents 0.2% of all adverse event reports for OLODATEROL\TIOTROPIUM.
9
Reports of Product administration error with OLODATEROL\TIOTROPIUM
0.2%
of all OLODATEROL\TIOTROPIUM reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product administration error From OLODATEROL\TIOTROPIUM?
Of the 9 reports, 1 (11.1%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OLODATEROL\TIOTROPIUM. However, 9 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which OLODATEROL\TIOTROPIUM Alternatives Have Lower Product administration error Risk?
OLODATEROL\TIOTROPIUM vs OLOPATADINE
OLODATEROL\TIOTROPIUM vs OLUTASIDENIB
OLODATEROL\TIOTROPIUM vs OMACETAXINE MEPESUCCINATE
OLODATEROL\TIOTROPIUM vs OMADACYCLINE
OLODATEROL\TIOTROPIUM vs OMALIZUMAB