2014-02-26 - Female - 18 Years old
900066309
| Adverse reaction report number | 900066309 |
| Latest AER version number | 0 |
| Market authorization holder AER number | ALL1-2014-01076 |
| Initial received date | 2014-02-26 |
| Latest received date | 2014-02-26 |
| Age | 18 Years |
| Gender | Female |
| Weight | N/A |
| Type of report | Spontaneous |
| Reporter type | Pharmacist |
| Source of report | MAH |
| Report outcome | Recovered/resolved |
| Serious report? | Yes |
Reason for seriousness
| Death | |
| Disability | |
| Cogenital anomaly | |
| Life threateting | |
| Hospitalization | |
| Other medically important | Yes |
| 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) | Product used for unknown indication | ||
| ADDERALL XR | CAPSULE, EXTENDED RELEASE | Suspect | Oral | 10 Milligram | 1 every 1 Day(s) | Product used for unknown indication |
| MedDRA version: v.21.1 | |
| Adverse reaction terms | Reaction duration |
|---|---|
| Blister | |
| Pain | |
| Skin discolouration | |