2017-07-04 - Unknown
901378371
| Adverse reaction report number | 901378371 |
| Latest AER version number | 0 |
| Market authorization holder AER number | CA201713968 |
| Initial received date | 2017-07-04 |
| Latest received date | 2017-07-04 |
| Age | N/A |
| Gender | Unknown |
| Weight | N/A |
| Type of report | Spontaneous |
| Reporter type | Consumer Or Other Non Health Professional |
| Source of report | MAH |
| Report outcome | Unknown |
| 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 | Unknown | Product used for unknown indication | |||
| MAS (MIXED AMPHETAMINE SALTS) | Concomitant | Unknown | Product used for unknown indication |
| MedDRA version: v.21.1 | |
| Adverse reaction terms | Reaction duration |
|---|---|
| Drug ineffective | |