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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does WATER Cause Incorrect product storage? 176 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 176 reports of Incorrect product storage have been filed in association with WATER (Sterile Diluent for Treprostinil). This represents 3.7% of all adverse event reports for WATER.

176
Reports of Incorrect product storage with WATER
3.7%
of all WATER reports
0
Deaths
1
Hospitalizations

How Dangerous Is Incorrect product storage From WATER?

Of the 176 reports, 1 (0.6%) required hospitalization.

Is Incorrect product storage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for WATER. However, 176 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) Herpes zoster (167) Product preparation error (165) Injection site pain (160) Death (129) Malaise (128) Product dose omission issue (115)

What Other Drugs Cause Incorrect product storage?

ETANERCEPT (2,149) INSULIN LISPRO (1,114) ABATACEPT (583) TERIPARATIDE (573) ADALIMUMAB (476) GOLIMUMAB (392) INSULIN GLARGINE (341) INSULIN HUMAN (336) USTEKINUMAB (299) ERYTHROPOIETIN (268)

Which WATER Alternatives Have Lower Incorrect product storage Risk?

WATER vs WELLBUTRIN WATER vs XALATAN WATER vs XALKORI WATER vs XANAX WATER vs XANTOFYL

Related Pages

WATER Full Profile All Incorrect product storage Reports All Drugs Causing Incorrect product storage WATER Demographics