Does ARTESUNATE Cause Condition aggravated? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Condition aggravated have been filed in association with ARTESUNATE. This represents 6.8% of all adverse event reports for ARTESUNATE.
11
Reports of Condition aggravated with ARTESUNATE
6.8%
of all ARTESUNATE reports
5
Deaths
7
Hospitalizations
How Dangerous Is Condition aggravated From ARTESUNATE?
Of the 11 reports, 5 (45.5%) resulted in death, 7 (63.6%) required hospitalization, and 1 (9.1%) 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 ARTESUNATE. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does ARTESUNATE Cause?
Haemolytic anaemia (48)
Drug ineffective (17)
Haemolysis (12)
Maternal exposure during pregnancy (11)
Off label use (11)
Acute kidney injury (7)
Agranulocytosis (7)
Drug interaction (7)
Exposure during pregnancy (7)
Hepatotoxicity (7)
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 ARTESUNATE Alternatives Have Lower Condition aggravated Risk?
ARTESUNATE vs ARTICAINE\EPINEPHRINE
ARTESUNATE vs ASCIMINIB
ARTESUNATE vs ASCORBIC ACID
ARTESUNATE vs ASCORBIC ACID\FERROUS
ARTESUNATE vs ASCORBIC ACID\FERROUS\FOLIC ACID