Does LEVOMILNACIPRAN Cause Product quality issue? 139 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 139 reports of Product quality issue have been filed in association with LEVOMILNACIPRAN (Fetzima). This represents 10.1% of all adverse event reports for LEVOMILNACIPRAN.
139
Reports of Product quality issue with LEVOMILNACIPRAN
10.1%
of all LEVOMILNACIPRAN reports
136
Deaths
82
Hospitalizations
How Dangerous Is Product quality issue From LEVOMILNACIPRAN?
Of the 139 reports, 136 (97.8%) resulted in death, 82 (59.0%) required hospitalization, and 83 (59.7%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVOMILNACIPRAN. However, 139 reports have been filed with the FAERS database.
What Other Side Effects Does LEVOMILNACIPRAN Cause?
Off label use (376)
Drug ineffective (315)
Gastrooesophageal reflux disease (295)
Vomiting (294)
Hypoaesthesia (290)
Abdominal pain upper (285)
Paraesthesia (282)
Memory impairment (277)
Blepharospasm (276)
Taste disorder (276)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which LEVOMILNACIPRAN Alternatives Have Lower Product quality issue Risk?
LEVOMILNACIPRAN vs LEVONORGESTREL
LEVOMILNACIPRAN vs LEVORPHANOL
LEVOMILNACIPRAN vs LEVOSIMENDAN
LEVOMILNACIPRAN vs LEVOSULPIRIDE
LEVOMILNACIPRAN vs LEVOTHYROXINE