FDA Drug Adverse Events (FAERS)

Report 26940628v1

Serious

Report Type: 1

Reported information does not establish causation. The fact that an adverse event has been reported does not mean that the suspect drug caused the adverse event. The event may have been related to the underlying disease, other concurrent medications, or other factors.

Received

2026-06-30T00:00:00.000Z

FDA receipt

2026-06-30T00:00:00.000Z

Drugs

Reactions

reported from JP

Patient information

Every demographic field FAERS publishes; most reports carry only some.

Age: 73 Years
Age Group: Elderly
Sex: Male
Weight (kg): Not reported

Outcome and seriousness

The seriousness criteria the reporter marked, as published.

Serious Outcome: Yes
Death: No
Hospitalization: No
Life Threatening: No
Disabling: No
Congenital Anomaly: No
Other Important: Yes

Reported drugs

Suspect, concomitant and interacting drugs, with the role the reporter gave each.

METGLUCOSuspect

METFORMIN HYDROCHLORIDE

Not Attempted

Clinical Use

IndicationDiabetes mellitus

Action Taken4

Administration Route

Not reported

Dosage Form

Not reported

Dosage Details

Not reported

Frequency

Not reported

Cumulative Dose

N/A

Reported reactions (MedDRA)

The reporter's own MedDRA preferred terms, with each term's outcome.

Glomerular filtration rate decreasedOutcome:UnknownUrine output decreasedOutcome:UnknownDiarrhoeaOutcome:Not recovered/not resolvedNauseaOutcome:Not recovered/not resolvedContraindicated product administeredUnknown

Source record

The FAERS payload this page was built from, exactly as it landed.

Historical FDA Source Record

Local Archive

Version: 1