Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122314283 | 12231428 | 3 | F | 20160617 | 20160401 | 20160829 | PER | US-TEVA-647059USA | TEVA | 0.00 | M | Y | 0.00000 | 20160830 | CN | US | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122314283 | 12231428 | 1 | PS | NUVIGIL | ARMODAFINIL | 1 | Unknown | 150 MILLIGRAM DAILY; | U | 21875 | 150 | MG | QD | ||||||
| 122314283 | 12231428 | 2 | SS | PROVIGIL | MODAFINIL | 1 | Unknown | 800 MILLIGRAM DAILY; | U | UNKNOWN | 20717 | 400 | MG | TABLET | BID |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122314283 | 12231428 | Asthenia | |
| 122314283 | 12231428 | Drug ineffective | |
| 122314283 | 12231428 | Fatigue | |
| 122314283 | 12231428 | Somnolence |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |