FDA Drug Adverse Events (FAERS)

Report 26940637v1

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 US

Patient information

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

Age: 62 Years
Age Group: Not reported
Sex: Female
Weight (kg): Not reported

Outcome and seriousness

The seriousness criteria the reporter marked, as published.

Serious Outcome: No

Reported drugs

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

TYMLOSSuspect

ABALOPARATIDE

Not Attempted

Clinical Use

IndicationProduct used for unknown indication

Action Taken5

Administration Route

Not reported

Dosage Form

Not reported

Dosage Details

80 MICROGRAM, QD

Frequency

Not reported

Cumulative Dose

N/A

Reported reactions (MedDRA)

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

ArthralgiaOutcome:Not recovered/not resolvedMood alteredOutcome:Not recovered/not resolvedIntentional dose omissionOutcome:UnknownProduct administered at inappropriate siteOutcome:Not recovered/not resolved

Source record

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

Historical FDA Source Record

Local Archive

Version: 1