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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127305091 | 12730509 | 1 | I | 20160715 | 20160909 | 20160909 | PER | US-TEVA-678757USA | TEVA | 0.00 | M | Y | 0.00000 | 20160910 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127305091 | 12730509 | 1 | PS | NUVIGIL | ARMODAFINIL | 1 | Unknown | 21875 | |||||||||||
| 127305091 | 12730509 | 2 | SS | PROVIGIL | MODAFINIL | 1 | Unknown | 20717 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127305091 | 12730509 | 1 | Multiple sclerosis |
| 127305091 | 12730509 | 2 | Multiple sclerosis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127305091 | 12730509 | Drug ineffective for unapproved indication | |
| 127305091 | 12730509 | Headache | |
| 127305091 | 12730509 | Intentional product use issue | |
| 127305091 | 12730509 | Product use issue | |
| 127305091 | 12730509 | Wrong technique in product usage process |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |