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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 TOFACITINIB Cause Postmenopausal haemorrhage? 16 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Postmenopausal haemorrhage have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.0% of all adverse event reports for TOFACITINIB.

16
Reports of Postmenopausal haemorrhage with TOFACITINIB
0.0%
of all TOFACITINIB reports
0
Deaths
3
Hospitalizations

How Dangerous Is Postmenopausal haemorrhage From TOFACITINIB?

Of the 16 reports, 3 (18.8%) required hospitalization.

Is Postmenopausal haemorrhage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 16 reports have been filed with the FAERS database.

What Other Side Effects Does TOFACITINIB Cause?

Drug ineffective (30,382) Pain (21,659) Condition aggravated (16,925) Arthralgia (15,640) Fatigue (13,551) Rheumatoid arthritis (12,277) Off label use (11,736) Headache (11,061) Joint swelling (10,686) Malaise (9,040)

What Other Drugs Cause Postmenopausal haemorrhage?

RIVAROXABAN (180) ESTRADIOL (160) ESTRADIOL\NORETHINDRONE (103) PROGESTERONE (78) TIRZEPATIDE (71) ASPIRIN (67) ADALIMUMAB (61) ESTRADIOL\LEVONORGESTREL (45) SEMAGLUTIDE (36) ESTROGENS, CONJUGATED\MEDROXYPROGESTERONE (34)

Which TOFACITINIB Alternatives Have Lower Postmenopausal haemorrhage Risk?

TOFACITINIB vs TOFERSEN TOFACITINIB vs TOLNAFTATE TOFACITINIB vs TOLODODEKIN ALFA TOFACITINIB vs TOLTERODINE TOFACITINIB vs TOLVAPTAN

Related Pages

TOFACITINIB Full Profile All Postmenopausal haemorrhage Reports All Drugs Causing Postmenopausal haemorrhage TOFACITINIB Demographics