2006-09-07 - Male
207594
| Adverse reaction report number | 207594 |
| Latest AER version number | 0 |
| Market authorization holder AER number | SPV1200600630 |
| Initial received date | 2006-09-07 |
| Latest received date | 2006-09-07 |
| Age | N/A |
| Gender | Male |
| 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 | CAPSULE, EXTENDED RELEASE | Suspect | Oral | 10 Milligram | 1 Year(s) | ||
| REACTINE | NOT SPECIFIED | Concomitant | Unknown |
| MedDRA version: v.21.1 | |
| Adverse reaction terms | Reaction duration |
|---|---|
| Alopecia | |