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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 CLADRIBINE Cause Condition aggravated? 95 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 95 reports of Condition aggravated have been filed in association with CLADRIBINE (Cladribine). This represents 1.3% of all adverse event reports for CLADRIBINE.

95
Reports of Condition aggravated with CLADRIBINE
1.3%
of all CLADRIBINE reports
6
Deaths
30
Hospitalizations

How Dangerous Is Condition aggravated From CLADRIBINE?

Of the 95 reports, 6 (6.3%) resulted in death, 30 (31.6%) required hospitalization, and 5 (5.3%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CLADRIBINE. However, 95 reports have been filed with the FAERS database.

What Other Side Effects Does CLADRIBINE Cause?

Fatigue (696) Headache (579) Lymphocyte count decreased (448) Multiple sclerosis relapse (404) Nausea (354) Pneumonia (318) White blood cell count decreased (311) Urinary tract infection (242) Pyrexia (207) Multiple sclerosis (206)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which CLADRIBINE Alternatives Have Lower Condition aggravated Risk?

CLADRIBINE vs CLARAVIS CLADRIBINE vs CLARITHROMYCIN CLADRIBINE vs CLARITIN CLADRIBINE vs CLARITIN CHEWABLE CLADRIBINE vs CLARITIN-D-12

Related Pages

CLADRIBINE Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated CLADRIBINE Demographics