2008-10-21 - Unknown
312848
| Adverse reaction report number | 312848 |
| Latest AER version number | 0 |
| Market authorization holder AER number | SPV1200802230 |
| Initial received date | 2008-10-21 |
| Latest received date | 2008-10-21 |
| Age | N/A |
| Gender | Unknown |
| Weight | N/A |
| Type of report | Spontaneous |
| Reporter type | Physician |
| Source of report | MAH |
| Report outcome | Recovered/resolved |
| Serious report? | No |
| Product description | Dosage form | Health product role | Route of administration | Dose | Frequency | Therapy duration | Indication(s) |
|---|---|---|---|---|---|---|---|
| ADDERALL XR | Suspect | Unknown | 25 Milligram | 1 every 1 Day(s) | Product used for unknown indication | ||
| ADDERALL XR | CAPSULE, EXTENDED RELEASE | Suspect | Unknown | 20 Milligram | 1 every 1 Day(s) | Product used for unknown indication |
| MedDRA version: v.21.1 | |
| Adverse reaction terms | Reaction duration |
|---|---|
| Aggression | |
| Drug ineffective | |