Does TESAMORELIN Cause Product dose omission? 53 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 53 reports of Product dose omission have been filed in association with TESAMORELIN (EGRIFTA SV). This represents 2.2% of all adverse event reports for TESAMORELIN.
53
Reports of Product dose omission with TESAMORELIN
2.2%
of all TESAMORELIN reports
0
Deaths
7
Hospitalizations
How Dangerous Is Product dose omission From TESAMORELIN?
Of the 53 reports, 7 (13.2%) required hospitalization, and 1 (1.9%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TESAMORELIN. However, 53 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 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 TESAMORELIN Alternatives Have Lower Product dose omission Risk?
TESAMORELIN vs TESTOSTERONE
TESAMORELIN vs TESTOSTERONE CYPIONATE
TESAMORELIN vs TESTOSTERONE ENANTHATE
TESAMORELIN vs TESTOSTERONE UNDECANOATE
TESAMORELIN vs TETANUS TOXOIDS