Does RAMELTEON Cause Wrong technique in product usage process? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Wrong technique in product usage process have been filed in association with RAMELTEON (Ramelteon). This represents 3.6% of all adverse event reports for RAMELTEON.
30
Reports of Wrong technique in product usage process with RAMELTEON
3.6%
of all RAMELTEON reports
1
Deaths
5
Hospitalizations
How Dangerous Is Wrong technique in product usage process From RAMELTEON?
Of the 30 reports, 1 (3.3%) resulted in death, 5 (16.7%) required hospitalization, and 1 (3.3%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RAMELTEON. However, 30 reports have been filed with the FAERS database.
What Other Side Effects Does RAMELTEON Cause?
Drug ineffective (160)
Somnolence (61)
Off label use (58)
Intentional overdose (45)
No adverse event (41)
Toxicity to various agents (41)
Dizziness (38)
Insomnia (30)
Overdose (28)
Nausea (27)
What Other Drugs Cause Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which RAMELTEON Alternatives Have Lower Wrong technique in product usage process Risk?
RAMELTEON vs RAMIPRIL
RAMELTEON vs RAMUCIRUMAB
RAMELTEON vs RANEXA
RAMELTEON vs RANIBIZUMAB
RAMELTEON vs RANIMUSTINE