2009-04-20 - Male - 41 Years old
322218
| Adverse reaction report number | 322218 |
| Latest AER version number | 1 |
| Market authorization holder AER number | SPV1200900648 |
| Initial received date | 2009-04-20 |
| Latest received date | 2009-05-07 |
| Age | 41 Years |
| Gender | Male |
| Weight | N/A |
| Type of report | Spontaneous |
| Reporter type | Consumer Or Other Non Health Professional |
| Source of report | MAH |
| Report outcome | Unknown |
| 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 | Unknown | 100 Milligram | every 1 Day(s) | Product used for unknown indication | ||
| ADDERALL XR | CAPSULE, EXTENDED RELEASE | Suspect | Unknown | 75 Milligram | every 1 Day(s) | Product used for unknown indication | |
| LITHIUM | NOT SPECIFIED | Concomitant | Unknown | ||||
| SEROQUEL | TABLET | Concomitant | Unknown | ||||
| WELLBUTRIN | TABLET (EXTENDED-RELEASE) | Concomitant | Unknown |
| MedDRA version: v.21.1 | |
| Adverse reaction terms | Reaction duration |
|---|---|
| Arthralgia | |
| Drug ineffective | |
| Inappropriate schedule of product administration | |
| Meniscus injury | |
| Prescribed overdose | |