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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122389382 | 12238938 | 2 | F | 20160606 | 20160405 | 20160706 | PER | US-PFIZER INC-2016146280 | PFIZER | 85.00 | YR | F | Y | 0.00000 | 20160706 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122389382 | 12238938 | 1 | PS | PROCARDIA | NIFEDIPINE | 1 | 60 MG, 1X/DAY | 18482 | 60 | MG | CAPSULE, SOFT | QD | |||||||
| 122389382 | 12238938 | 2 | SS | PROCARDIA | NIFEDIPINE | 1 | 60 MG, UNK (1X) | L51560 | 18482 | 60 | MG | CAPSULE, SOFT | |||||||
| 122389382 | 12238938 | 3 | SS | LOSARTAN. | LOSARTAN | 1 | 100 MG, 1X/DAY | 0 | 100 | MG | QD | ||||||||
| 122389382 | 12238938 | 4 | SS | LOSARTAN. | LOSARTAN | 1 | 20 MG, UNK (1X) | 0 | 20 | MG | |||||||||
| 122389382 | 12238938 | 5 | C | ARIMIDEX | ANASTROZOLE | 1 | 1 MG, UNK | 0 | 1 | MG | |||||||||
| 122389382 | 12238938 | 6 | C | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | 50 MG, UNK | 0 | 50 | MG | |||||||||
| 122389382 | 12238938 | 7 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | 12.5 MG, UNK | 0 | 12.5 | MG | |||||||||
| 122389382 | 12238938 | 8 | C | POTASSIUM | POTASSIUM | 1 | UNK | 0 | |||||||||||
| 122389382 | 12238938 | 9 | C | ASPIRIN. | ASPIRIN | 1 | 81 MG, UNK | 0 | 81 | MG | |||||||||
| 122389382 | 12238938 | 10 | C | TURMERIC | TURMERIC | 1 | 1000 MG, UNK | 0 | 1000 | MG | |||||||||
| 122389382 | 12238938 | 11 | C | PROBIOTIC | PROBIOTICS NOS | 1 | UNK (2X) | 0 | |||||||||||
| 122389382 | 12238938 | 12 | C | MAGNESIUM | MAGNESIUM | 1 | 400 MG, UNK | 0 | 400 | MG | |||||||||
| 122389382 | 12238938 | 13 | C | VITAMIN D3 | CHOLECALCIFEROL | 1 | 2000 IU, UNK | 0 | 2000 | IU | |||||||||
| 122389382 | 12238938 | 14 | C | COQ10 | UBIDECARENONE | 1 | 200 MG, UNK | 0 | 200 | MG | |||||||||
| 122389382 | 12238938 | 15 | C | RANITIDINE. | RANITIDINE | 1 | 75 MG, UNK (75MG 2X) | 0 | 75 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122389382 | 12238938 | 1 | Blood pressure measurement |
| 122389382 | 12238938 | 2 | Hypertension |
| 122389382 | 12238938 | 3 | Blood pressure measurement |
| 122389382 | 12238938 | 4 | Hypertension |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122389382 | 12238938 | Blood pressure inadequately controlled |
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 |
|---|---|---|---|---|---|---|
| 122389382 | 12238938 | 1 | 201511 | 0 | ||
| 122389382 | 12238938 | 2 | 201509 | 0 | ||
| 122389382 | 12238938 | 3 | 201511 | 0 | ||
| 122389382 | 12238938 | 4 | 201603 | 201604 | 0 |