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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127080371 | 12708037 | 1 | I | 20130918 | 20130927 | 20160901 | 20160901 | EXP | US-PFIZER INC-2013279949 | PFIZER | 69.00 | YR | F | Y | 88.40000 | KG | 20160901 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127080371 | 12708037 | 1 | SS | NAPROXEN. | NAPROXEN | 1 | Oral | UNK | 0 | TABLET | |||||||||
| 127080371 | 12708037 | 2 | SS | NAPROXEN. | NAPROXEN | 1 | 0 | TABLET | |||||||||||
| 127080371 | 12708037 | 3 | PS | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | Oral | 50 MG, QD | 28850 | MG | 74133 | 50 | MG | QD | |||||
| 127080371 | 12708037 | 4 | SS | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | Oral | 50 MG, ONCE DAILY | 28850 | MG | 74133 | 50 | MG | QD | |||||
| 127080371 | 12708037 | 5 | C | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | Oral | 20 MG, QD | 0 | 20 | MG | QD | |||||||
| 127080371 | 12708037 | 6 | C | ASPIRIN. | ASPIRIN | 1 | Oral | 325 MG, QD | 0 | 325 | MG | QD | |||||||
| 127080371 | 12708037 | 7 | C | ZOLOFT | SERTRALINE HYDROCHLORIDE | 1 | Oral | 50 MG, QD | 0 | 50 | MG | QD | |||||||
| 127080371 | 12708037 | 8 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | Oral | 12.5 MG, QD | 0 | 12.5 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127080371 | 12708037 | 1 | Osteoarthritis |
| 127080371 | 12708037 | 2 | Rheumatoid arthritis |
| 127080371 | 12708037 | 3 | Hypertension |
| 127080371 | 12708037 | 5 | Prophylaxis |
| 127080371 | 12708037 | 6 | Coronary artery disease |
| 127080371 | 12708037 | 7 | Antidepressant therapy |
| 127080371 | 12708037 | 8 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127080371 | 12708037 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127080371 | 12708037 | Atrial fibrillation | |
| 127080371 | 12708037 | Syncope |
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 |
|---|---|---|---|---|---|---|
| 127080371 | 12708037 | 1 | 20110227 | 20131113 | 0 | |
| 127080371 | 12708037 | 3 | 20120219 | 20130917 | 0 | |
| 127080371 | 12708037 | 4 | 20130918 | 0 | ||
| 127080371 | 12708037 | 5 | 20110227 | 0 | ||
| 127080371 | 12708037 | 7 | 2009 | 0 | ||
| 127080371 | 12708037 | 8 | 20120110 | 0 |