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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125053612 | 12505361 | 2 | F | 20160816 | 20160628 | 20160822 | PER | US-PFIZER INC-2016295207 | PFIZER | 75.00 | YR | F | Y | 98.43000 | KG | 20160822 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125053612 | 12505361 | 1 | PS | LYRICA | PREGABALIN | 1 | Oral | 50 MG, EVERY 8 HOURS, 3X/DAY | M90071 | 21446 | 50 | MG | TID | ||||||
| 125053612 | 12505361 | 2 | SS | PERCOCET | ACETAMINOPHENOXYCODONE HYDROCHLORIDE | 1 | U | 0 | |||||||||||
| 125053612 | 12505361 | 3 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 1 DF, 1 TABLET | 0 | 1 | DF | TABLET | ||||||||
| 125053612 | 12505361 | 4 | C | ASPIRIN. | ASPIRIN | 1 | 81 MG, UNK | 0 | 81 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125053612 | 12505361 | 1 | Herpes zoster |
| 125053612 | 12505361 | 2 | Herpes zoster |
| 125053612 | 12505361 | 4 | Prophylaxis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125053612 | 12505361 | Drug ineffective |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 125053612 | 12505361 | 1 | 20160607 | 0 |