2010-10-18 - Female - 36 Years old
353502
| Adverse reaction report number | 353502 |
| Latest AER version number | 0 |
| Market authorization holder AER number | N/A |
| Initial received date | 2010-10-18 |
| Latest received date | 2010-10-18 |
| Age | 36 Years |
| Gender | Female |
| Weight | 119 Pounds |
| Type of report | Spontaneous |
| Reporter type | Pharmacist |
| Source of report | Community |
| Report outcome | Unknown |
| Serious report? | No |
| Product description | Dosage form | Health product role | Route of administration | Dose | Frequency | Therapy duration | Indication(s) |
|---|---|---|---|---|---|---|---|
| ADDERALL XR 20MG | CAPSULE, EXTENDED RELEASE | Suspect | Oral | 20 Milligram | 1 every 1 Day(s) | Attention deficit/hyperactivity disorder | |
| AMOXICILLIN | NOT SPECIFIED | Concomitant | Oral | ||||
| NASONEX | SPRAY (NOT INHALATION) | Concomitant | Intra-nasal | ||||
| PMS-CLONAZEPAM | TABLET | Concomitant | |||||
| SYNTHROID | NOT SPECIFIED | Concomitant | Oral | ||||
| ZOPICLONE | TABLET | Concomitant | Oral |
| MedDRA version: v.21.1 | |
| Adverse reaction terms | Reaction duration |
|---|---|
| Anxiety | |
| Insomnia | |
| Nervousness | |
| Psychomotor hyperactivity | |