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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 THALIDOMIDE Cause International normalised ratio increased? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of International normalised ratio increased have been filed in association with THALIDOMIDE (Thalomid). This represents 0.0% of all adverse event reports for THALIDOMIDE.

6
Reports of International normalised ratio increased with THALIDOMIDE
0.0%
of all THALIDOMIDE reports
1
Deaths
4
Hospitalizations

How Dangerous Is International normalised ratio increased From THALIDOMIDE?

Of the 6 reports, 1 (16.7%) resulted in death, 4 (66.7%) required hospitalization.

Is International normalised ratio increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for THALIDOMIDE. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does THALIDOMIDE Cause?

Plasma cell myeloma (1,652) Off label use (1,356) Death (1,161) Neuropathy peripheral (1,068) Drug ineffective (789) Pneumonia (694) Fatigue (643) Constipation (461) Thrombocytopenia (429) Neutropenia (420)

What Other Drugs Cause International normalised ratio increased?

WARFARIN (5,622) RIVAROXABAN (863) ACETAMINOPHEN (533) ASPIRIN (448) APIXABAN (317) CLOPIDOGREL BISULFATE (314) FLUINDIONE (286) AMIODARONE (277) FUROSEMIDE (277) DABIGATRAN ETEXILATE (223)

Which THALIDOMIDE Alternatives Have Lower International normalised ratio increased Risk?

THALIDOMIDE vs THALOMID THALIDOMIDE vs THEOPHYLLINE THALIDOMIDE vs THEOPHYLLINE ANHYDROUS THALIDOMIDE vs THIAMINE THALIDOMIDE vs THIOCOLCHICOSIDE

Related Pages

THALIDOMIDE Full Profile All International normalised ratio increased Reports All Drugs Causing International normalised ratio increased THALIDOMIDE Demographics