Does TESAMORELIN Cause Product storage error? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Product storage error have been filed in association with TESAMORELIN (EGRIFTA SV). This represents 1.1% of all adverse event reports for TESAMORELIN.
27
Reports of Product storage error with TESAMORELIN
1.1%
of all TESAMORELIN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product storage error From TESAMORELIN?
Of the 27 reports, 1 (3.7%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TESAMORELIN. However, 27 reports have been filed with the FAERS database.
What Other Side Effects Does TESAMORELIN Cause?
Product dose omission issue (277)
Arthralgia (188)
Injection site pain (186)
Incorrect dose administered (167)
Drug ineffective (159)
Weight increased (138)
Injection site bruising (134)
Peripheral swelling (126)
Pain in extremity (121)
Product preparation issue (119)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which TESAMORELIN Alternatives Have Lower Product storage error Risk?
TESAMORELIN vs TESTOSTERONE
TESAMORELIN vs TESTOSTERONE CYPIONATE
TESAMORELIN vs TESTOSTERONE ENANTHATE
TESAMORELIN vs TESTOSTERONE UNDECANOATE
TESAMORELIN vs TETANUS TOXOIDS