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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 100163633 | 10016363 | 3 | F | 201403 | 20140623 | 20140317 | 20140630 | PER | US-PFIZER INC-2014076488 | PFIZER | 51.00 | YR | F | Y | 95.24000 | KG | 20140629 | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 100163633 | 10016363 | 1 | PS | Lyrica | 1 | 300 MG, 2X/DAY | D | 21446 | 300 | MG | BID | ||||||||
| 100163633 | 10016363 | 2 | C | TYSABRI | 1 | UNK, EVERY 4 WEEKS | D | 0 | |||||||||||
| 100163633 | 10016363 | 3 | C | LISINOPRIL | 1 | 20 MG, DAILY | D | 0 | 20 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 100163633 | 10016363 | 1 | Fibromyalgia |
| 100163633 | 10016363 | 2 | Multiple sclerosis |
| 100163633 | 10016363 | 3 | Hypertension |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 100163633 | 10016363 | Contusion | |
| 100163633 | 10016363 | Fall | |
| 100163633 | 10016363 | Joint injury |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |