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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 SARILUMAB Cause Intentional dose omission? 67 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 67 reports of Intentional dose omission have been filed in association with SARILUMAB (KEVZARA). This represents 0.3% of all adverse event reports for SARILUMAB.

67
Reports of Intentional dose omission with SARILUMAB
0.3%
of all SARILUMAB reports
5
Deaths
8
Hospitalizations

How Dangerous Is Intentional dose omission From SARILUMAB?

Of the 67 reports, 5 (7.5%) resulted in death, 8 (11.9%) required hospitalization, and 3 (4.5%) were considered life-threatening.

Is Intentional dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SARILUMAB. However, 67 reports have been filed with the FAERS database.

What Other Side Effects Does SARILUMAB Cause?

Drug ineffective (5,065) Pain (4,833) Arthralgia (4,139) Rheumatoid arthritis (3,963) Joint swelling (3,951) Condition aggravated (3,247) Fatigue (3,000) Rash (2,912) Alopecia (2,660) Abdominal discomfort (2,600)

What Other Drugs Cause Intentional dose omission?

DUPILUMAB (2,269) CERTOLIZUMAB PEGOL (1,253) ADALIMUMAB (845) TOFACITINIB (845) INFLIXIMAB (815) ABALOPARATIDE (623) ETANERCEPT (615) AMBRISENTAN (595) SODIUM OXYBATE (580) CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)

Which SARILUMAB Alternatives Have Lower Intentional dose omission Risk?

SARILUMAB vs SATRALIZUMAB SARILUMAB vs SATRALIZUMAB-MWGE SARILUMAB vs SAXAGLIPTIN SARILUMAB vs SCHOLL'S INGROWN TOENAIL PAIN RELIEVER SARILUMAB vs SCOPOLAMINE

Related Pages

SARILUMAB Full Profile All Intentional dose omission Reports All Drugs Causing Intentional dose omission SARILUMAB Demographics