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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ORLISTAT Cause Product quality issue? 453 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 453 reports of Product quality issue have been filed in association with ORLISTAT (Xenical). This represents 7.0% of all adverse event reports for ORLISTAT.

453
Reports of Product quality issue with ORLISTAT
7.0%
of all ORLISTAT reports
1
Deaths
0
Hospitalizations

How Dangerous Is Product quality issue From ORLISTAT?

Of the 453 reports, 1 (0.2%) resulted in death.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ORLISTAT. However, 453 reports have been filed with the FAERS database.

What Other Side Effects Does ORLISTAT Cause?

Drug ineffective (2,329) Steatorrhoea (681) Diarrhoea (562) Treatment noncompliance (517) Rectal discharge (475) Weight increased (320) Abdominal pain upper (314) Flatulence (231) Constipation (225) Faeces discoloured (203)

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 ORLISTAT Alternatives Have Lower Product quality issue Risk?

ORLISTAT vs ORNIDAZOLE ORLISTAT vs ORPHENADRINE ORLISTAT vs OSELTAMIVIR ORLISTAT vs OSILODROSTAT ORLISTAT vs OSIMERTINIB

Related Pages

ORLISTAT Full Profile All Product quality issue Reports All Drugs Causing Product quality issue ORLISTAT Demographics