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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 Product packaging quantity issue? 62 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 62 reports of Product packaging quantity issue have been filed in association with WATER (Sterile Diluent for Treprostinil). This represents 1.3% of all adverse event reports for WATER.

62
Reports of Product packaging quantity issue with WATER
1.3%
of all WATER reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product packaging quantity issue From WATER?

Of the 62 reports.

Is Product packaging quantity issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for WATER. However, 62 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) Product preparation error (165) Injection site pain (160) Death (129) Malaise (128)

What Other Drugs Cause Product packaging quantity issue?

LEUPROLIDE (523) ALBUTEROL (431) BUDESONIDE\FORMOTEROL (301) FENTANYL (286) BUPRENORPHINE (225) CYCLOSPORINE (206) ESTRADIOL (201) BIMATOPROST (177) RIVAROXABAN (174) EXENATIDE (154)

Which WATER Alternatives Have Lower Product packaging quantity issue Risk?

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

Related Pages

WATER Full Profile All Product packaging quantity issue Reports All Drugs Causing Product packaging quantity issue WATER Demographics