Does NALTREXONE Cause Wrong technique in product usage process? 443 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 443 reports of Wrong technique in product usage process have been filed in association with NALTREXONE (NALTREXONE HYDROCHLORIDE). This represents 1.7% of all adverse event reports for NALTREXONE.
443
Reports of Wrong technique in product usage process with NALTREXONE
1.7%
of all NALTREXONE reports
0
Deaths
15
Hospitalizations
How Dangerous Is Wrong technique in product usage process From NALTREXONE?
Of the 443 reports, 15 (3.4%) required hospitalization.
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 NALTREXONE. However, 443 reports have been filed with the FAERS database.
What Other Side Effects Does NALTREXONE Cause?
Injection site reaction (4,360)
Injection site pain (2,990)
Alcoholism (1,928)
Injection site mass (1,849)
Nausea (1,782)
Fatigue (1,486)
Pain (1,348)
Drug dependence (1,334)
Drug ineffective (1,250)
Feeling abnormal (1,241)
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 NALTREXONE Alternatives Have Lower Wrong technique in product usage process Risk?
NALTREXONE vs NAPHAZOLINE\PHENIRAMINE
NALTREXONE vs NAPROXEN
NALTREXONE vs NAPROXEN\NAPROXEN
NALTREXONE vs NAPROXEN\PSEUDOEPHEDRINE
NALTREXONE vs NAPROXEN\SUMATRIPTAN