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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 TRIPROLIDINE Cause Condition aggravated? 29 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Condition aggravated have been filed in association with TRIPROLIDINE (Childrens PediaClear PD). This represents 17.1% of all adverse event reports for TRIPROLIDINE.

29
Reports of Condition aggravated with TRIPROLIDINE
17.1%
of all TRIPROLIDINE reports
19
Deaths
19
Hospitalizations

How Dangerous Is Condition aggravated From TRIPROLIDINE?

Of the 29 reports, 19 (65.5%) resulted in death, 19 (65.5%) required hospitalization, and 29 (100.0%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TRIPROLIDINE. However, 29 reports have been filed with the FAERS database.

What Other Side Effects Does TRIPROLIDINE Cause?

Psoriatic arthropathy (110) Type 2 diabetes mellitus (109) Pericarditis (108) Joint swelling (106) Oedema (106) Pemphigus (105) Pyrexia (105) Sinusitis (104) Urticaria (103) Injury (102)

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 TRIPROLIDINE Alternatives Have Lower Condition aggravated Risk?

TRIPROLIDINE vs TRIPTORELIN TRIPROLIDINE vs TRISODIUM TRIPROLIDINE vs TROFINETIDE TRIPROLIDINE vs TROFOSFAMIDE TRIPROLIDINE vs TROPATEPINE

Related Pages

TRIPROLIDINE Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated TRIPROLIDINE Demographics