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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 112351293 | 11235129 | 3 | F | 201506 | 20160727 | 20150702 | 20160817 | PER | US-PFIZER INC-2015217776 | PFIZER | 66.00 | YR | M | Y | 124.00000 | KG | 20160817 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 112351293 | 11235129 | 1 | PS | PROCARDIA XL | NIFEDIPINE | 1 | Oral | 90 MG, 1X/DAY | 19684 | 90 | MG | MODIFIED-RELEASE TABLET | QD | ||||||
| 112351293 | 11235129 | 2 | SS | PROCARDIA XL | NIFEDIPINE | 1 | Oral | 60 MG, 1X/DAY | 19684 | 60 | MG | MODIFIED-RELEASE TABLET | QD | ||||||
| 112351293 | 11235129 | 3 | SS | VIAGRA | SILDENAFIL CITRATE | 1 | UNK | 20895 | FILM-COATED TABLET | ||||||||||
| 112351293 | 11235129 | 4 | C | POTASSIUM | POTASSIUM | 1 | Oral | 20 MG, 1X/DAY | 0 | 20 | MG | TABLET | QD | ||||||
| 112351293 | 11235129 | 5 | C | HCTZ | HYDROCHLOROTHIAZIDE | 1 | 25 MG, 1X/DAY | 0 | 25 | MG | TABLET | QD | |||||||
| 112351293 | 11235129 | 6 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | 25 MG, 1X/DAY | 0 | 25 | MG | TABLET | QD | |||||||
| 112351293 | 11235129 | 7 | C | TAMSULOSIN HCL | TAMSULOSIN | 1 | 0.4 MG, 1X/DAY | 0 | .4 | MG | CAPSULE | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 112351293 | 11235129 | 5 | Fluid retention |
| 112351293 | 11235129 | 6 | Restless legs syndrome |
| 112351293 | 11235129 | 7 | Fluid retention |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 112351293 | 11235129 | Back disorder | |
| 112351293 | 11235129 | Sciatica |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |