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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 ALLANTOIN Cause Cardiogenic shock? 94 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 94 reports of Cardiogenic shock have been filed in association with ALLANTOIN (TriDerma Aloe Zinc Occlusive). This represents 59.9% of all adverse event reports for ALLANTOIN.

94
Reports of Cardiogenic shock with ALLANTOIN
59.9%
of all ALLANTOIN reports
94
Deaths
62
Hospitalizations

How Dangerous Is Cardiogenic shock From ALLANTOIN?

Of the 94 reports, 94 (100.0%) resulted in death, 62 (66.0%) required hospitalization, and 62 (66.0%) were considered life-threatening.

Is Cardiogenic shock Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALLANTOIN. However, 94 reports have been filed with the FAERS database.

What Other Side Effects Does ALLANTOIN Cause?

Hyponatraemia (108) Condition aggravated (107) General physical health deterioration (105) Stress (105) Multiple organ dysfunction syndrome (104) Sepsis (103) Somnolence (103) Abdominal distension (101) Vomiting (100) Off label use (99)

What Other Drugs Cause Cardiogenic shock?

AMLODIPINE (779) AMIODARONE (595) BUPROPION (559) ACETAMINOPHEN (466) METOPROLOL (454) BISOPROLOL (413) VERAPAMIL (412) NOREPINEPHRINE (381) HEPARIN (357) METFORMIN (356)

Which ALLANTOIN Alternatives Have Lower Cardiogenic shock Risk?

ALLANTOIN vs ALLEGRA ALLANTOIN vs ALLEGRA 24 HOUR ALLANTOIN vs ALLEGRA D ALLANTOIN vs ALLERGENIC EXTRACT- PEANUT ARACHIS HYPOGAEA ALLANTOIN vs ALLERGENIC EXTRACTS

Related Pages

ALLANTOIN Full Profile All Cardiogenic shock Reports All Drugs Causing Cardiogenic shock ALLANTOIN Demographics