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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 PLECANATIDE Cause Intentional product misuse? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Intentional product misuse have been filed in association with PLECANATIDE (Trulance Immediate release). This represents 0.7% of all adverse event reports for PLECANATIDE.

7
Reports of Intentional product misuse with PLECANATIDE
0.7%
of all PLECANATIDE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Intentional product misuse From PLECANATIDE?

Of the 7 reports, 1 (14.3%) required hospitalization.

Is Intentional product misuse Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PLECANATIDE. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does PLECANATIDE Cause?

Diarrhoea (298) Drug ineffective (100) Constipation (92) Abdominal distension (83) Nausea (72) Abdominal pain (71) Abdominal pain upper (70) Flatulence (58) Product use in unapproved indication (51) Muscle spasms (49)

What Other Drugs Cause Intentional product misuse?

ETANERCEPT (3,992) PREGABALIN (3,731) BUDESONIDE\FORMOTEROL (3,399) ACETAMINOPHEN (2,924) ESOMEPRAZOLE (2,852) MINOXIDIL (2,418) TOFACITINIB (2,331) CINACALCET (2,092) QUETIAPINE (1,855) ALPRAZOLAM (1,709)

Which PLECANATIDE Alternatives Have Lower Intentional product misuse Risk?

PLECANATIDE vs PLERIXAFOR PLECANATIDE vs PNEUMOCOCCAL 13-VALENT CONJUGATE VACCINE PLECANATIDE vs PNEUMOCOCCAL 7-VALENT CONJUGATE VACCINE PLECANATIDE vs PNEUMOCOCCAL VACCINE POLYVALENT PLECANATIDE vs PNEUMOCOCCAL VACCINE, POLYVALENT 23

Related Pages

PLECANATIDE Full Profile All Intentional product misuse Reports All Drugs Causing Intentional product misuse PLECANATIDE Demographics