2013-05-15 - Male - 49 Years old
526503
| Adverse reaction report number | 526503 |
| Latest AER version number | 0 |
| Market authorization holder AER number | ALL1201302834 |
| Initial received date | 2013-05-15 |
| Latest received date | 2013-05-15 |
| Age | 49 Years |
| Gender | Male |
| Weight | N/A |
| Type of report | Spontaneous |
| Reporter type | Pharmacist |
| 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) |
|---|---|---|---|---|---|---|---|
| ADDERALL XR | Suspect | Oral | 20 Milligram | 1 every 1 Day(s) | Attention deficit/hyperactivity disorder | ||
| ADDERALL XR | CAPSULE, EXTENDED RELEASE | Suspect | Oral | 20 Milligram | 2 every 1 Day(s) | Attention deficit/hyperactivity disorder |
| MedDRA version: v.21.1 | |
| Adverse reaction terms | Reaction duration |
|---|---|
| Drug effect decreased | |
| Off label use | |
| Overdose | |