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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 Low density lipoprotein increased? 135 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 135 reports of Low density lipoprotein increased have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.1% of all adverse event reports for TOFACITINIB.

135
Reports of Low density lipoprotein increased with TOFACITINIB
0.1%
of all TOFACITINIB reports
0
Deaths
6
Hospitalizations

How Dangerous Is Low density lipoprotein increased From TOFACITINIB?

Of the 135 reports, 6 (4.4%) required hospitalization, and 1 (0.7%) were considered life-threatening.

Is Low density lipoprotein increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 135 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 Low density lipoprotein increased?

EVOLOCUMAB (1,024) INCLISIRAN (423) ALIROCUMAB (336) ROSUVASTATIN (241) ATORVASTATIN (217) EZETIMIBE (217) LOMITAPIDE (164) FINGOLIMOD (132) SOMATROPIN (93) LORLATINIB (78)

Which TOFACITINIB Alternatives Have Lower Low density lipoprotein increased Risk?

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

Related Pages

TOFACITINIB Full Profile All Low density lipoprotein increased Reports All Drugs Causing Low density lipoprotein increased TOFACITINIB Demographics