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Aptivus (Tipranavir) - Side Effect Reports to FDA

 
 



This is an index of side effect / adverse reaction reports (a.k.a. adverse event reports) related to Aptivus (Tipranavir) and submitted to the FDA during the sample period of about a year. The information is not vetted and should not be considered as verified clinical evidence.

Reports by Event Outcome

All Cases (2)

Reports by Reaction Type

Pallor (1)Dyspnoea Exertional (1)Retinal Degeneration (1)Anaemia (1)

Possible Aptivus side effects in male

Reported by a health professional (non-physician/pharmacist) from France on 2012-05-15

Patient: male

Reactions: Dyspnoea Exertional, Anaemia, Pallor

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Aptivus
    Administration route: Oral
    Indication: HIV Infection CDC Category A3
    Start date: 2009-01-16
    End date: 2012-01-09

Combivir
    Indication: HIV Infection CDC Category A3
    Start date: 2011-09-23
    End date: 2012-01-02

Other drugs received by patient: Intelence; Norvir



Possible Aptivus side effects in

Reported by a pharmacist from United States on 2011-12-06

Patient:

Reactions: Retinal Degeneration

Drug(s) suspected as cause:
Aptivus

Viread

Epivir

Isentress

Norvir

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