Does COMBIVENT Cause Product quality issue? 385 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 385 reports of Product quality issue have been filed in association with COMBIVENT. This represents 30.8% of all adverse event reports for COMBIVENT.
385
Reports of Product quality issue with COMBIVENT
30.8%
of all COMBIVENT reports
0
Deaths
35
Hospitalizations
How Dangerous Is Product quality issue From COMBIVENT?
Of the 385 reports, 35 (9.1%) 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 COMBIVENT. However, 385 reports have been filed with the FAERS database.
What Other Side Effects Does COMBIVENT Cause?
Off label use (311)
Dyspnoea (262)
Drug ineffective (257)
Cough (107)
Overdose (103)
Prescribed overdose (73)
Pneumonia (47)
Drug prescribing error (39)
Choking (33)
Wheezing (32)
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 COMBIVENT Alternatives Have Lower Product quality issue Risk?
COMBIVENT vs COMBIVIR
COMBIVENT vs COMETRIQ
COMBIVENT vs CONCERTA
COMBIVENT vs CONESTAT ALFA
COMBIVENT vs COPANLISIB