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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 Blood test abnormal? 30 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Blood test abnormal have been filed in association with ALLANTOIN (TriDerma Aloe Zinc Occlusive). This represents 19.1% of all adverse event reports for ALLANTOIN.

30
Reports of Blood test abnormal with ALLANTOIN
19.1%
of all ALLANTOIN reports
30
Deaths
29
Hospitalizations

How Dangerous Is Blood test abnormal From ALLANTOIN?

Of the 30 reports, 30 (100.0%) resulted in death, 29 (96.7%) required hospitalization, and 29 (96.7%) were considered life-threatening.

Is Blood test abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALLANTOIN. However, 30 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 Blood test abnormal?

ALBUTEROL (1,075) LENALIDOMIDE (857) ADALIMUMAB (675) PREDNISONE (659) MONTELUKAST (618) BUDESONIDE\FORMOTEROL (587) PALBOCICLIB (533) LEVOTHYROXINE (500) METHOTREXATE (418) TRAZODONE (407)

Which ALLANTOIN Alternatives Have Lower Blood test abnormal 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 Blood test abnormal Reports All Drugs Causing Blood test abnormal ALLANTOIN Demographics