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Aptivus (Tipranavir) - Side Effect Reports to FDA

 
 



Index of reports > All Cases (2)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Aptivus (Tipranavir) all cases. The selected reports were submitted to the FDA during the sample period of about a year.

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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