Does ALLI Cause Product quality issue? 125 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 125 reports of Product quality issue have been filed in association with ALLI. This represents 11.8% of all adverse event reports for ALLI.
125
Reports of Product quality issue with ALLI
11.8%
of all ALLI reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product quality issue From ALLI?
Of the 125 reports, 1 (0.8%) 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 ALLI. However, 125 reports have been filed with the FAERS database.
What Other Side Effects Does ALLI Cause?
Drug ineffective (332)
Treatment noncompliance (233)
Rectal discharge (183)
Steatorrhoea (182)
Diarrhoea (118)
Weight increased (90)
Drug administration error (81)
Constipation (69)
Frequent bowel movements (66)
Abdominal pain upper (65)
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 ALLI Alternatives Have Lower Product quality issue Risk?
ALLI vs ALLOPURINOL
ALLI vs ALMOTRIPTAN
ALLI vs ALMOTRIPTAN MALATE
ALLI vs ALOE VERA LEAF
ALLI vs ALOGLIPTIN