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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125833911 | 12583391 | 1 | I | 20160510 | 20160713 | 20160722 | 20160722 | EXP | GB-PFIZER INC-2016350488 | PFIZER | 81.00 | YR | F | Y | 0.00000 | 20160722 | PH | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125833911 | 12583391 | 1 | PS | RAMIPRIL. | RAMIPRIL | 1 | Oral | 10 MG, DAILY | Y | 19901 | 10 | MG | CAPSULE | ||||||
| 125833911 | 12583391 | 2 | SS | RAMIPRIL. | RAMIPRIL | 1 | Oral | 5 MG, DAILY | Y | 19901 | 5 | MG | CAPSULE | ||||||
| 125833911 | 12583391 | 3 | C | ASPIRIN /00002701/ | ASPIRIN | 1 | UNK | 0 | |||||||||||
| 125833911 | 12583391 | 4 | C | ATORVASTATIN | ATORVASTATIN | 1 | UNK | 0 | |||||||||||
| 125833911 | 12583391 | 5 | C | BISOPROLOL | BISOPROLOL | 1 | UNK | 0 | |||||||||||
| 125833911 | 12583391 | 6 | C | COLECALCIFEROL | CHOLECALCIFEROL | 1 | UNK | 0 | |||||||||||
| 125833911 | 12583391 | 7 | C | FERROUS FUMARATE | FERROUS FUMARATE | 1 | UNK | 0 | |||||||||||
| 125833911 | 12583391 | 8 | C | FUROSEMIDE. | FUROSEMIDE | 1 | UNK | 0 | |||||||||||
| 125833911 | 12583391 | 9 | C | GLICLAZIDE | GLICLAZIDE | 1 | UNK | 0 | |||||||||||
| 125833911 | 12583391 | 10 | C | ISOSORBIDE MONONITRATE. | ISOSORBIDE MONONITRATE | 1 | UNK | 0 | |||||||||||
| 125833911 | 12583391 | 11 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 125833911 | 12583391 | 12 | C | NICORANDIL | NICORANDIL | 1 | UNK | 0 | |||||||||||
| 125833911 | 12583391 | 13 | C | RANITIDINE. | RANITIDINE | 1 | UNK | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125833911 | 12583391 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125833911 | 12583391 | Dizziness | |
| 125833911 | 12583391 | Dyspnoea | |
| 125833911 | 12583391 | Dyspnoea exertional | |
| 125833911 | 12583391 | Hypotension |
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 |
|---|---|---|---|---|---|---|
| 125833911 | 12583391 | 1 | 20160510 | 0 |