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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125706641 | 12570664 | 1 | I | 20160705 | 20160719 | 20160719 | PER | US-PFIZER INC-2016332497 | PFIZER | 0.00 | F | Y | 0.00000 | 20160719 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125706641 | 12570664 | 1 | PS | XANAX | ALPRAZOLAM | 1 | UNK | U | 18276 | ||||||||||
| 125706641 | 12570664 | 2 | I | NORCO | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Oral | HYDROCODONE BITARTRATE 10 MG, PARACETAMOL 325 MG (3 TO 4 TIMES DAILY), AS NEEDED | U | 0 | |||||||||
| 125706641 | 12570664 | 3 | C | ALEVE | NAPROXEN SODIUM | 1 | UNK | 0 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125706641 | 12570664 | Drug ineffective | |
| 125706641 | 12570664 | Drug interaction | |
| 125706641 | 12570664 | Feeling abnormal | |
| 125706641 | 12570664 | Headache | |
| 125706641 | 12570664 | Panic attack | |
| 125706641 | 12570664 | Restlessness | |
| 125706641 | 12570664 | Tremor |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |