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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127034191 | 12703419 | 1 | I | 20160826 | 20160831 | 20160831 | PER | US-PFIZER INC-2016407700 | PFIZER | 0.00 | Y | 0.00000 | 20160831 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127034191 | 12703419 | 1 | PS | LYRICA | PREGABALIN | 1 | 50 MG, 2X/DAY | U | 21446 | 50 | MG | BID | |||||||
| 127034191 | 12703419 | 2 | SS | LYRICA | PREGABALIN | 1 | 150 MG, 3X/DAY | U | 21446 | 150 | MG | TID | |||||||
| 127034191 | 12703419 | 3 | SS | HYDROCODONE | HYDROCODONE | 1 | UNK | U | 0 | ||||||||||
| 127034191 | 12703419 | 4 | SS | TYLENOL | ACETAMINOPHEN | 1 | 325 MG, UNK | U | 0 | 325 | MG | ||||||||
| 127034191 | 12703419 | 5 | SS | MOTRIN | IBUPROFEN | 1 | 800 MG, UNK | 0 | 800 | MG | |||||||||
| 127034191 | 12703419 | 6 | SS | NORCO | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | AS NEEDED (3 TIMES) | 0 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127034191 | 12703419 | Condition aggravated | |
| 127034191 | 12703419 | Pain | |
| 127034191 | 12703419 | Rash |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |