2009-05-26 - Male
324291
| Adverse reaction report number | 324291 |
| Latest AER version number | 0 |
| Market authorization holder AER number | 2009-04-21 |
| Initial received date | 2009-05-26 |
| Latest received date | 2009-05-26 |
| Age | N/A |
| Gender | Male |
| Weight | N/A |
| Type of report | Study |
| Reporter type | Consumer Or Other Non Health Professional |
| Source of report | MAH |
| Report outcome | Not recovered/not resolved |
| Serious report? | No |
| Product description | Dosage form | Health product role | Route of administration | Dose | Frequency | Therapy duration | Indication(s) |
|---|---|---|---|---|---|---|---|
| COMBIVIR | TABLET | Suspect | Unknown | HIV infection | |||
| KALETRA | NOT SPECIFIED | Suspect | Unknown | HIV infection | |||
| TRUVADA | TABLET | Suspect | Unknown | HIV infection | |||
| VIRAMUNE | TABLET | Suspect | Unknown | HIV infection |
| MedDRA version: v.21.1 | |
| Adverse reaction terms | Reaction duration |
|---|---|
| Abdominal pain | |
| Confusional state | |
| Diarrhoea | |
| Fatigue | |
| Liver disorder | |
| Nausea | |