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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does NALOXONE\TILIDINE Cause Hypersensitivity? 17 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Hypersensitivity have been filed in association with NALOXONE\TILIDINE. This represents 2.6% of all adverse event reports for NALOXONE\TILIDINE.

17
Reports of Hypersensitivity with NALOXONE\TILIDINE
2.6%
of all NALOXONE\TILIDINE reports
0
Deaths
17
Hospitalizations

How Dangerous Is Hypersensitivity From NALOXONE\TILIDINE?

Of the 17 reports, 17 (100.0%) required hospitalization.

Is Hypersensitivity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NALOXONE\TILIDINE. However, 17 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 Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Which NALOXONE\TILIDINE Alternatives Have Lower Hypersensitivity Risk?

NALOXONE\TILIDINE vs NALTREXONE NALOXONE\TILIDINE vs NAPHAZOLINE\PHENIRAMINE NALOXONE\TILIDINE vs NAPROXEN NALOXONE\TILIDINE vs NAPROXEN\NAPROXEN NALOXONE\TILIDINE vs NAPROXEN\PSEUDOEPHEDRINE

Related Pages

NALOXONE\TILIDINE Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity NALOXONE\TILIDINE Demographics