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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 Condition aggravated? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Condition aggravated have been filed in association with NALOXONE\TILIDINE. This represents 1.2% of all adverse event reports for NALOXONE\TILIDINE.

8
Reports of Condition aggravated with NALOXONE\TILIDINE
1.2%
of all NALOXONE\TILIDINE reports
0
Deaths
3
Hospitalizations

How Dangerous Is Condition aggravated From NALOXONE\TILIDINE?

Of the 8 reports, 3 (37.5%) required hospitalization.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NALOXONE\TILIDINE. However, 8 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which NALOXONE\TILIDINE Alternatives Have Lower Condition aggravated 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 Condition aggravated Reports All Drugs Causing Condition aggravated NALOXONE\TILIDINE Demographics