Does METRELEPTIN Cause Product storage error? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product storage error have been filed in association with METRELEPTIN (Myalept). This represents 0.6% of all adverse event reports for METRELEPTIN.
7
Reports of Product storage error with METRELEPTIN
0.6%
of all METRELEPTIN reports
1
Deaths
4
Hospitalizations
How Dangerous Is Product storage error From METRELEPTIN?
Of the 7 reports, 1 (14.3%) resulted in death, 4 (57.1%) required hospitalization, and 1 (14.3%) were considered life-threatening.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METRELEPTIN. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does METRELEPTIN Cause?
Therapy cessation (94)
Product dose omission issue (88)
Weight decreased (88)
Blood glucose increased (77)
Drug ineffective (69)
Therapy interrupted (65)
Nausea (57)
Off label use (51)
Blood triglycerides increased (49)
Treatment noncompliance (49)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which METRELEPTIN Alternatives Have Lower Product storage error Risk?
METRELEPTIN vs METRONIDAZOLE
METRELEPTIN vs METRONIDAZOLE\METRONIDAZOLE
METRELEPTIN vs METYRAPONE
METRELEPTIN vs MEXILETINE
METRELEPTIN vs MIANSERIN