Does SETMELANOTIDE Cause Product dose omission in error? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product dose omission in error have been filed in association with SETMELANOTIDE (Imcivree). This represents 5.0% of all adverse event reports for SETMELANOTIDE.
9
Reports of Product dose omission in error with SETMELANOTIDE
5.0%
of all SETMELANOTIDE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission in error From SETMELANOTIDE?
Of the 9 reports, 3 (33.3%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SETMELANOTIDE. However, 9 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 Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which SETMELANOTIDE Alternatives Have Lower Product dose omission in error Risk?
SETMELANOTIDE vs SEVELAMER
SETMELANOTIDE vs SEVOFLURANE
SETMELANOTIDE vs SIBUTRAMINE
SETMELANOTIDE vs SILDENAFIL
SETMELANOTIDE vs SILODOSIN