Does NALOXONE\TILIDINE Cause Product administration error? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Product administration error have been filed in association with NALOXONE\TILIDINE. This represents 2.4% of all adverse event reports for NALOXONE\TILIDINE.
16
Reports of Product administration error with NALOXONE\TILIDINE
2.4%
of all NALOXONE\TILIDINE reports
0
Deaths
16
Hospitalizations
How Dangerous Is Product administration error From NALOXONE\TILIDINE?
Of the 16 reports, 16 (100.0%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NALOXONE\TILIDINE. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does NALOXONE\TILIDINE Cause?
Fall (186)
Dizziness (126)
Pain (98)
Nausea (83)
Constipation (80)
Fatigue (77)
General physical health deterioration (76)
Vomiting (71)
Arthralgia (69)
Abdominal pain upper (56)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which NALOXONE\TILIDINE Alternatives Have Lower Product administration error Risk?
NALOXONE\TILIDINE vs NALTREXONE
NALOXONE\TILIDINE vs NAPHAZOLINE\PHENIRAMINE
NALOXONE\TILIDINE vs NAPROXEN
NALOXONE\TILIDINE vs NAPROXEN\NAPROXEN
NALOXONE\TILIDINE vs NAPROXEN\PSEUDOEPHEDRINE