Does ASFOTASE ALFA Cause Condition aggravated? 105 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 105 reports of Condition aggravated have been filed in association with ASFOTASE ALFA (STRENSIQ). This represents 1.2% of all adverse event reports for ASFOTASE ALFA.
105
Reports of Condition aggravated with ASFOTASE ALFA
1.2%
of all ASFOTASE ALFA reports
3
Deaths
13
Hospitalizations
How Dangerous Is Condition aggravated From ASFOTASE ALFA?
Of the 105 reports, 3 (2.9%) resulted in death, 13 (12.4%) required hospitalization, and 4 (3.8%) 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 ASFOTASE ALFA. However, 105 reports have been filed with the FAERS database.
What Other Side Effects Does ASFOTASE ALFA Cause?
Injection site pain (1,227)
Injection site erythema (828)
Fatigue (759)
Pain (673)
Injection site reaction (659)
Arthralgia (524)
Injection site bruising (469)
Pain in extremity (463)
Injection site swelling (417)
Headache (322)
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 ASFOTASE ALFA Alternatives Have Lower Condition aggravated Risk?
ASFOTASE ALFA vs ASIAN GINSENG
ASFOTASE ALFA vs ASMANEX TWISTHALER
ASFOTASE ALFA vs ASPARAGINASE
ASFOTASE ALFA vs ASPARAGINASE ERWINIA CHRYSANTHEMI
ASFOTASE ALFA vs ASPARAGINASE ERWINIA CHRYSANTHEMI -RYWN