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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125366732 | 12536673 | 2 | F | 20160719 | 20160707 | 20160725 | EXP | US-PFIZER INC-2016327679 | PFIZER | 0.00 | F | Y | 0.00000 | 20160725 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125366732 | 12536673 | 1 | PS | XANAX | ALPRAZOLAM | 1 | 1 MG, UNK | U | M26070 | 18276 | 1 | MG | TABLET |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125366732 | 12536673 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125366732 | 12536673 | Abdominal discomfort | |
| 125366732 | 12536673 | Anxiety | |
| 125366732 | 12536673 | Chest discomfort | |
| 125366732 | 12536673 | Drug ineffective | |
| 125366732 | 12536673 | Fatigue | |
| 125366732 | 12536673 | Feeling abnormal | |
| 125366732 | 12536673 | Product colour issue | |
| 125366732 | 12536673 | Rash | |
| 125366732 | 12536673 | Rash macular | |
| 125366732 | 12536673 | Somnolence | |
| 125366732 | 12536673 | Throat tightness | |
| 125366732 | 12536673 | Urticaria |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |