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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127909031 | 12790903 | 1 | I | 20160607 | 20160915 | 20160929 | 20160929 | EXP | GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-124394 | RANBAXY | 77.00 | YR | M | Y | 0.00000 | 20160929 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127909031 | 12790903 | 1 | PS | Atorvastatin | ATORVASTATIN | 1 | Oral | 10 MG, QD, AT NIGHT | Y | U | 76477 | 10 | MG | ||||||
| 127909031 | 12790903 | 2 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 20 MG, QD, EACH MORNING | 0 | 20 | MG | ||||||||
| 127909031 | 12790903 | 3 | SS | RAMIPRIL. | RAMIPRIL | 1 | Oral | 10 MG, QD, EVERY MORNING | Y | U | 0 | 10 | MG | ||||||
| 127909031 | 12790903 | 4 | C | ADCAL-D3 | CALCIUM CARBONATECHOLECALCIFEROL | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 127909031 | 12790903 | 5 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 127909031 | 12790903 | 6 | C | ATENOLOL. | ATENOLOL | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 127909031 | 12790903 | 7 | C | BISACODYL. | BISACODYL | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 127909031 | 12790903 | 8 | C | CARMELLOSE | 2 | Unknown | UNK | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127909031 | 12790903 | 1 | Hypercholesterolaemia |
| 127909031 | 12790903 | 2 | Oedema peripheral |
| 127909031 | 12790903 | 3 | Hypertension |
| 127909031 | 12790903 | 4 | Product used for unknown indication |
| 127909031 | 12790903 | 5 | Product used for unknown indication |
| 127909031 | 12790903 | 6 | Product used for unknown indication |
| 127909031 | 12790903 | 7 | Product used for unknown indication |
| 127909031 | 12790903 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127909031 | 12790903 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127909031 | 12790903 | Acute kidney injury | |
| 127909031 | 12790903 | Asthenia | |
| 127909031 | 12790903 | Dizziness | |
| 127909031 | 12790903 | Dyspnoea | |
| 127909031 | 12790903 | Fall | |
| 127909031 | 12790903 | Hyponatraemia | |
| 127909031 | 12790903 | 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 |
|---|---|---|---|---|---|---|
| 127909031 | 12790903 | 1 | 20160609 | 0 |