Does OLODATEROL\TIOTROPIUM Cause Product quality issue? 167 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 167 reports of Product quality issue have been filed in association with OLODATEROL\TIOTROPIUM. This represents 3.8% of all adverse event reports for OLODATEROL\TIOTROPIUM.
167
Reports of Product quality issue with OLODATEROL\TIOTROPIUM
3.8%
of all OLODATEROL\TIOTROPIUM reports
0
Deaths
15
Hospitalizations
How Dangerous Is Product quality issue From OLODATEROL\TIOTROPIUM?
Of the 167 reports, 15 (9.0%) required hospitalization.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OLODATEROL\TIOTROPIUM. However, 167 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which OLODATEROL\TIOTROPIUM Alternatives Have Lower Product quality issue Risk?
OLODATEROL\TIOTROPIUM vs OLOPATADINE
OLODATEROL\TIOTROPIUM vs OLUTASIDENIB
OLODATEROL\TIOTROPIUM vs OMACETAXINE MEPESUCCINATE
OLODATEROL\TIOTROPIUM vs OMADACYCLINE
OLODATEROL\TIOTROPIUM vs OMALIZUMAB