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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127499591 | 12749959 | 1 | I | 20160818 | 20160905 | 20160916 | 20160916 | EXP | GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-123978 | RANBAXY | 87.00 | YR | F | Y | 59.60000 | KG | 20160916 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127499591 | 12749959 | 1 | PS | Zoledronic acid | ZOLEDRONIC ACID | 1 | Intravenous (not otherwise specified) | 1 DF, UNK | U | 202746 | 1 | DF | |||||||
| 127499591 | 12749959 | 2 | C | AMITRIPTYLINE | AMITRIPTYLINE | 1 | Unknown | U | U | 0 | |||||||||
| 127499591 | 12749959 | 3 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | U | U | 0 | |||||||||
| 127499591 | 12749959 | 4 | C | COCODAMOL | ACETAMINOPHENCODEINE PHOSPHATE | 1 | Unknown | U | U | 0 | |||||||||
| 127499591 | 12749959 | 5 | C | COLECALCIFEROL | CHOLECALCIFEROL | 1 | Unknown | U | U | 0 | |||||||||
| 127499591 | 12749959 | 6 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127499591 | 12749959 | 1 | Osteoporosis |
| 127499591 | 12749959 | 2 | Product used for unknown indication |
| 127499591 | 12749959 | 3 | Product used for unknown indication |
| 127499591 | 12749959 | 4 | Product used for unknown indication |
| 127499591 | 12749959 | 5 | Product used for unknown indication |
| 127499591 | 12749959 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127499591 | 12749959 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127499591 | 12749959 | Atrial fibrillation | |
| 127499591 | 12749959 | Chest discomfort | |
| 127499591 | 12749959 | Dyspnoea | |
| 127499591 | 12749959 | Malaise | |
| 127499591 | 12749959 | Palpitations |
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 |
|---|---|---|---|---|---|---|
| 127499591 | 12749959 | 1 | 20160816 | 20160816 | 0 |