Does ESKETAMINE Cause Device issue? 210 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 210 reports of Device issue have been filed in association with ESKETAMINE (Spravato). This represents 1.4% of all adverse event reports for ESKETAMINE.
210
Reports of Device issue with ESKETAMINE
1.4%
of all ESKETAMINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device issue From ESKETAMINE?
Of the 210 reports.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ESKETAMINE. However, 210 reports have been filed with the FAERS database.
What Other Side Effects Does ESKETAMINE Cause?
Dissociation (3,103)
Sedation (2,244)
Suicidal ideation (1,254)
Drug ineffective (1,005)
Nausea (807)
Depression (800)
Anxiety (659)
Hospitalisation (657)
Product dose omission issue (635)
Hypertension (605)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which ESKETAMINE Alternatives Have Lower Device issue Risk?
ESKETAMINE vs ESLICARBAZEPINE
ESKETAMINE vs ESMOLOL
ESKETAMINE vs ESOMEPRAZOLE
ESKETAMINE vs ESOMEPRAZOLE\ESOMEPRAZOLE\ESOMEPRAZOLE
ESKETAMINE vs ESOMEPRAZOLE\NAPROXEN