Does TESTOSTERONE CYPIONATE Cause Product dose omission issue? 209 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 209 reports of Product dose omission issue have been filed in association with TESTOSTERONE CYPIONATE (Testosterone Cypionate). This represents 4.0% of all adverse event reports for TESTOSTERONE CYPIONATE.
209
Reports of Product dose omission issue with TESTOSTERONE CYPIONATE
4.0%
of all TESTOSTERONE CYPIONATE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product dose omission issue From TESTOSTERONE CYPIONATE?
Of the 209 reports, 1 (0.5%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TESTOSTERONE CYPIONATE. However, 209 reports have been filed with the FAERS database.
What Other Side Effects Does TESTOSTERONE CYPIONATE Cause?
Myocardial infarction (929)
Cerebrovascular accident (663)
Deep vein thrombosis (611)
Pulmonary embolism (552)
Drug ineffective (345)
Thrombosis (325)
Product deposit (287)
Pain (281)
Poor quality product administered (235)
Anxiety (234)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which TESTOSTERONE CYPIONATE Alternatives Have Lower Product dose omission issue Risk?
TESTOSTERONE CYPIONATE vs TESTOSTERONE ENANTHATE
TESTOSTERONE CYPIONATE vs TESTOSTERONE UNDECANOATE
TESTOSTERONE CYPIONATE vs TETANUS TOXOIDS
TESTOSTERONE CYPIONATE vs TETRABENAZINE
TESTOSTERONE CYPIONATE vs TETRACAINE