Does TESAMORELIN Cause Product preparation issue? 119 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 119 reports of Product preparation issue have been filed in association with TESAMORELIN (EGRIFTA SV). This represents 4.9% of all adverse event reports for TESAMORELIN.
119
Reports of Product preparation issue with TESAMORELIN
4.9%
of all TESAMORELIN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product preparation issue From TESAMORELIN?
Of the 119 reports, 2 (1.7%) required hospitalization.
Is Product preparation issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TESAMORELIN. However, 119 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)
Injection site pruritus (117)
What Other Drugs Cause Product preparation issue?
ONABOTULINUMTOXINA (677)
COAGULATION FACTOR IX HUMAN\COAGULATION FACTOR VII HUMAN\COAGULATION FACTOR X HUMAN\PROTEIN C\PROTEIN S HUMAN\PROTHROMBIN (252)
HUMAN C1-ESTERASE INHIBITOR (238)
SOMATROPIN (200)
INCOBOTULINUMTOXINA (174)
STIRIPENTOL (129)
ABATACEPT (115)
INFLIXIMAB (101)
ABOBOTULINUMTOXINA (91)
WATER (82)
Which TESAMORELIN Alternatives Have Lower Product preparation issue Risk?
TESAMORELIN vs TESTOSTERONE
TESAMORELIN vs TESTOSTERONE CYPIONATE
TESAMORELIN vs TESTOSTERONE ENANTHATE
TESAMORELIN vs TESTOSTERONE UNDECANOATE
TESAMORELIN vs TETANUS TOXOIDS