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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127728071 | 12772807 | 1 | I | 20160607 | 20160914 | 20160922 | 20160922 | EXP | GB-MHRA-EYC 00145051 | PHHY2016GB127218 | SANDOZ | 77.00 | YR | M | Y | 0.00000 | 20160922 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127728071 | 12772807 | 1 | PS | ATORVASTATIN | ATORVASTATIN | 1 | Oral | 10 MG, QD (AT NIGHT) | Y | U | 77575 | 10 | MG | QD | |||||
| 127728071 | 12772807 | 2 | SS | RAMIPRIL. | RAMIPRIL | 1 | Oral | 10 MG, QD (EVERY MORNING) | Y | U | 0 | 10 | MG | QD | |||||
| 127728071 | 12772807 | 3 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 20 MG, QD (EVERY MORNING) | 0 | 20 | MG | QD | |||||||
| 127728071 | 12772807 | 4 | C | ADCAL-D3 | CALCIUM CARBONATECHOLECALCIFEROL | 1 | Unknown | U | 0 | ||||||||||
| 127728071 | 12772807 | 5 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | U | 0 | ||||||||||
| 127728071 | 12772807 | 6 | C | ATENOLOL. | ATENOLOL | 1 | Unknown | U | 0 | ||||||||||
| 127728071 | 12772807 | 7 | C | BISACODYL. | BISACODYL | 1 | Unknown | U | 0 | ||||||||||
| 127728071 | 12772807 | 8 | C | CARMELLOSE | 2 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127728071 | 12772807 | 1 | Hypercholesterolaemia |
| 127728071 | 12772807 | 2 | Hypertension |
| 127728071 | 12772807 | 3 | Oedema peripheral |
| 127728071 | 12772807 | 4 | Product used for unknown indication |
| 127728071 | 12772807 | 5 | Product used for unknown indication |
| 127728071 | 12772807 | 6 | Product used for unknown indication |
| 127728071 | 12772807 | 7 | Product used for unknown indication |
| 127728071 | 12772807 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127728071 | 12772807 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127728071 | 12772807 | Acute kidney injury | |
| 127728071 | 12772807 | Asthenia | |
| 127728071 | 12772807 | Dizziness | |
| 127728071 | 12772807 | Dyspnoea | |
| 127728071 | 12772807 | Fall | |
| 127728071 | 12772807 | Hyponatraemia | |
| 127728071 | 12772807 | Rhabdomyolysis |
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 |
|---|---|---|---|---|---|---|
| 127728071 | 12772807 | 1 | 20160609 | 0 |