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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 GIVOSIRAN Cause Condition aggravated? 18 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Condition aggravated have been filed in association with GIVOSIRAN (GIVLAARI). This represents 1.5% of all adverse event reports for GIVOSIRAN.

18
Reports of Condition aggravated with GIVOSIRAN
1.5%
of all GIVOSIRAN reports
0
Deaths
9
Hospitalizations

How Dangerous Is Condition aggravated From GIVOSIRAN?

Of the 18 reports, 9 (50.0%) required hospitalization, and 1 (5.6%) 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 GIVOSIRAN. However, 18 reports have been filed with the FAERS database.

What Other Side Effects Does GIVOSIRAN Cause?

Porphyria acute (381) Hospitalisation (141) Nausea (91) Product dose omission issue (85) Fatigue (84) Therapy interrupted (83) Pain (74) Intentional dose omission (63) Abdominal pain (62) Vomiting (58)

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 GIVOSIRAN Alternatives Have Lower Condition aggravated Risk?

GIVOSIRAN vs GLASDEGIB GIVOSIRAN vs GLATIRAMER GIVOSIRAN vs GLECAPREVIR\PIBRENTASVIR GIVOSIRAN vs GLEEVEC GIVOSIRAN vs GLICLAZIDE

Related Pages

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