2014-12-09 - Unknown
900193632
| Adverse reaction report number | 900193632 |
| Latest AER version number | 0 |
| Market authorization holder AER number | CA201408789 |
| Initial received date | 2014-12-09 |
| Latest received date | 2014-12-09 |
| Age | N/A |
| Gender | Unknown |
| Weight | N/A |
| Type of report | Spontaneous |
| Reporter type | Pharmacist |
| 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 | Oral | 20 Milligram | Product used for unknown indication | ||
| CALCIUM CARBONATE | Concomitant | Unknown | Product used for unknown indication |
| MedDRA version: v.21.1 | |
| Adverse reaction terms | Reaction duration |
|---|---|
| Drug ineffective | |