Does TRIPROLIDINE Cause Intentional product use issue? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Intentional product use issue have been filed in association with TRIPROLIDINE (Childrens PediaClear PD). This represents 16.5% of all adverse event reports for TRIPROLIDINE.
28
Reports of Intentional product use issue with TRIPROLIDINE
16.5%
of all TRIPROLIDINE reports
18
Deaths
18
Hospitalizations
How Dangerous Is Intentional product use issue From TRIPROLIDINE?
Of the 28 reports, 18 (64.3%) resulted in death, 18 (64.3%) required hospitalization, and 28 (100.0%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TRIPROLIDINE. However, 28 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which TRIPROLIDINE Alternatives Have Lower Intentional product use issue Risk?
TRIPROLIDINE vs TRIPTORELIN
TRIPROLIDINE vs TRISODIUM
TRIPROLIDINE vs TROFINETIDE
TRIPROLIDINE vs TROFOSFAMIDE
TRIPROLIDINE vs TROPATEPINE