Does TESAMORELIN Cause Product administration error? 34 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Product administration error have been filed in association with TESAMORELIN (EGRIFTA SV). This represents 1.4% of all adverse event reports for TESAMORELIN.
34
Reports of Product administration error with TESAMORELIN
1.4%
of all TESAMORELIN reports
1
Deaths
2
Hospitalizations
How Dangerous Is Product administration error From TESAMORELIN?
Of the 34 reports, 1 (2.9%) resulted in death, 2 (5.9%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TESAMORELIN. However, 34 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which TESAMORELIN Alternatives Have Lower Product administration error Risk?
TESAMORELIN vs TESTOSTERONE
TESAMORELIN vs TESTOSTERONE CYPIONATE
TESAMORELIN vs TESTOSTERONE ENANTHATE
TESAMORELIN vs TESTOSTERONE UNDECANOATE
TESAMORELIN vs TETANUS TOXOIDS