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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 Intentional dose omission? 63 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 63 reports of Intentional dose omission have been filed in association with GIVOSIRAN (GIVLAARI). This represents 5.2% of all adverse event reports for GIVOSIRAN.

63
Reports of Intentional dose omission with GIVOSIRAN
5.2%
of all GIVOSIRAN reports
0
Deaths
48
Hospitalizations

How Dangerous Is Intentional dose omission From GIVOSIRAN?

Of the 63 reports, 48 (76.2%) required hospitalization.

Is Intentional dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GIVOSIRAN. However, 63 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) Abdominal pain (62) Vomiting (58) Malaise (56)

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 GIVOSIRAN Alternatives Have Lower Intentional dose omission Risk?

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

Related Pages

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