Does WATER Cause Product preparation error? 165 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 165 reports of Product preparation error have been filed in association with WATER (Sterile Diluent for Treprostinil). This represents 3.5% of all adverse event reports for WATER.
165
Reports of Product preparation error with WATER
3.5%
of all WATER reports
1
Deaths
3
Hospitalizations
How Dangerous Is Product preparation error From WATER?
Of the 165 reports, 1 (0.6%) resulted in death, 3 (1.8%) required hospitalization, and 12 (7.3%) were considered life-threatening.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for WATER. However, 165 reports have been filed with the FAERS database.
What Other Side Effects Does WATER Cause?
No adverse event (1,883)
Product storage error (656)
Expired product administered (399)
Pyrexia (189)
Incorrect product storage (176)
Herpes zoster (167)
Injection site pain (160)
Death (129)
Malaise (128)
Product dose omission issue (115)
What Other Drugs Cause Product preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)