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side effects patient, 62 years of age, was diagnosed with rash, antiviral prophylaxis, nausea and took Fenistil (nch)(dimetindene maleate) ampoule 1 Df, Tid; Intra. View more Serious Adverse Events reported to FDA.

List of Fenistil (nch)(dimetindene Maleate) Ampoule Adverse Effects reported to US Food and Drug Administration (FDA)

Stevens-johnson Syndrome, Toxic Epidermal Necrolysis (5646787-1)
on Feb 22, 2008 Male patient from GERMANY , 62 years of age, was diagnosed with
  • rash
and was treated with Fenistil (nch)(dimetindene Maleate) Ampoule. Patient experienced the following unwanted or unexpected effects: stevens-johnson syndrome, toxic epidermal necrolysis. Fenistil (nch)(dimetindene Maleate) Ampoule dosage: 1 Df, Tid; Intravenous, 1 Df, Tid, Intravenous. Patient was hospitalized.

Stevens-johnson Syndrome, Toxic Epidermal Necrolysis (5635635-1)
Patient was taking Fenistil (nch)(dimetindene Maleate) Ampoule. Patient had the following side effects: stevens-johnson syndrome, toxic epidermal necrolysis on Feb 04, 2008 from GERMANY Additional patient health information: Male patient , 62 years of age, was diagnosed with
  • rash
and. Fenistil (nch)(dimetindene Maleate) Ampoule dosage: 1 Df, Tid, Intravenous. Patient was hospitalized.

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Fenistil (nch)(dimetindene Maleate) Ampoule Information

More About Fenistil (nch)(dimetindene maleate) ampoule

Side Effects reported to FDA: 2. View FDA Adverse Reports

Fenistil (nch)(dimetindene Maleate) Ampoule safety alerts: No

Reported deaths: 2

Reported hospitalizations: 2

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Fenistil (nch)(dimetindene Maleate) Ampoule Adverse Reactions

Stevens-johnson Syndrome ( 2 Reports)

Toxic Epidermal Necrolysis ( 2 Reports)

side effects
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