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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 NATEGLINIDE Cause Product quality issue? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product quality issue have been filed in association with NATEGLINIDE (Nateglinide). This represents 4.9% of all adverse event reports for NATEGLINIDE.

9
Reports of Product quality issue with NATEGLINIDE
4.9%
of all NATEGLINIDE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product quality issue From NATEGLINIDE?

Of the 9 reports.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NATEGLINIDE. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does NATEGLINIDE Cause?

Drug ineffective (26) Blood glucose increased (17) Lactic acidosis (16) Toxicity to various agents (16) Hypoglycaemia (15) Blood glucose decreased (12) Glycosylated haemoglobin increased (11) Diarrhoea (10) Renal failure (10) Blood glucose fluctuation (8)

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 NATEGLINIDE Alternatives Have Lower Product quality issue Risk?

NATEGLINIDE vs NAVITOCLAX NATEGLINIDE vs NAXITAMAB-GQGK NATEGLINIDE vs NEBIVOLOL NATEGLINIDE vs NECITUMUMAB NATEGLINIDE vs NEDAPLATIN

Related Pages

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