Does ASFOTASE ALFA Cause Product dose omission? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Product dose omission have been filed in association with ASFOTASE ALFA (STRENSIQ). This represents 0.3% of all adverse event reports for ASFOTASE ALFA.
27
Reports of Product dose omission with ASFOTASE ALFA
0.3%
of all ASFOTASE ALFA reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission From ASFOTASE ALFA?
Of the 27 reports.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ASFOTASE ALFA. However, 27 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 Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which ASFOTASE ALFA Alternatives Have Lower Product dose omission 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