Does BUPRENORPHINE Cause Incorrect product administration duration? 129 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 129 reports of Incorrect product administration duration have been filed in association with BUPRENORPHINE (Buprenorphine and Naloxone). This represents 0.2% of all adverse event reports for BUPRENORPHINE.
129
Reports of Incorrect product administration duration with BUPRENORPHINE
0.2%
of all BUPRENORPHINE reports
68
Deaths
76
Hospitalizations
How Dangerous Is Incorrect product administration duration From BUPRENORPHINE?
Of the 129 reports, 68 (52.7%) resulted in death, 76 (58.9%) required hospitalization, and 64 (49.6%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUPRENORPHINE. However, 129 reports have been filed with the FAERS database.
What Other Side Effects Does BUPRENORPHINE Cause?
Drug dependence (16,730)
Overdose (13,977)
Death (13,604)
Toxicity to various agents (10,906)
Pain (8,219)
Drug withdrawal syndrome (7,149)
Emotional distress (6,159)
Drug abuse (4,344)
Drug ineffective (4,261)
Dependence (3,184)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which BUPRENORPHINE Alternatives Have Lower Incorrect product administration duration Risk?
BUPRENORPHINE vs BUPRENORPHINE\NALOXONE
BUPRENORPHINE vs BUPROPION
BUPRENORPHINE vs BUPROPION HYDROBROMIDE
BUPRENORPHINE vs BUPROPION\DEXTROMETHORPHAN HYDROBROMIDE
BUPRENORPHINE vs BUPROPION\NALTREXONE