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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 GLIMEPIRIDE Cause Hyperthyroidism? 79 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 79 reports of Hyperthyroidism have been filed in association with GLIMEPIRIDE (Glimepiride). This represents 1.4% of all adverse event reports for GLIMEPIRIDE.

79
Reports of Hyperthyroidism with GLIMEPIRIDE
1.4%
of all GLIMEPIRIDE reports
35
Deaths
39
Hospitalizations

How Dangerous Is Hyperthyroidism From GLIMEPIRIDE?

Of the 79 reports, 35 (44.3%) resulted in death, 39 (49.4%) required hospitalization, and 34 (43.0%) were considered life-threatening.

Is Hyperthyroidism Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GLIMEPIRIDE. However, 79 reports have been filed with the FAERS database.

What Other Side Effects Does GLIMEPIRIDE Cause?

Hypoglycaemia (1,403) Blood glucose increased (446) Acute kidney injury (339) Drug ineffective (339) Diarrhoea (257) Blood glucose decreased (232) Lactic acidosis (219) Glycosylated haemoglobin increased (214) Diabetes mellitus inadequate control (213) Hypoglycaemic coma (187)

What Other Drugs Cause Hyperthyroidism?

LEVOTHYROXINE (1,681) AMIODARONE (1,410) NIVOLUMAB (934) PEMBROLIZUMAB (780) IPILIMUMAB (525) CARBOPLATIN (432) ATEZOLIZUMAB (416) PACLITAXEL (261) ALEMTUZUMAB (236) LENVATINIB (231)

Which GLIMEPIRIDE Alternatives Have Lower Hyperthyroidism Risk?

GLIMEPIRIDE vs GLIMEPIRIDE\ROSIGLITAZONE GLIMEPIRIDE vs GLIPIZIDE GLIMEPIRIDE vs GLIVEC GLIMEPIRIDE vs GLOFITAMAB GLIMEPIRIDE vs GLOFITAMAB-GXBM

Related Pages

GLIMEPIRIDE Full Profile All Hyperthyroidism Reports All Drugs Causing Hyperthyroidism GLIMEPIRIDE Demographics