Does SETMELANOTIDE Cause Intentional dose omission? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Intentional dose omission have been filed in association with SETMELANOTIDE (Imcivree). This represents 4.4% of all adverse event reports for SETMELANOTIDE.
8
Reports of Intentional dose omission with SETMELANOTIDE
4.4%
of all SETMELANOTIDE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Intentional dose omission From SETMELANOTIDE?
Of the 8 reports, 4 (50.0%) 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 SETMELANOTIDE. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does SETMELANOTIDE Cause?
Nausea (53)
Off label use (48)
Skin hyperpigmentation (43)
Headache (27)
Skin discolouration (26)
Diarrhoea (24)
Vomiting (24)
Fatigue (23)
Decreased appetite (19)
Injection site pruritus (19)
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 SETMELANOTIDE Alternatives Have Lower Intentional dose omission Risk?
SETMELANOTIDE vs SEVELAMER
SETMELANOTIDE vs SEVOFLURANE
SETMELANOTIDE vs SIBUTRAMINE
SETMELANOTIDE vs SILDENAFIL
SETMELANOTIDE vs SILODOSIN