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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127399971 | 12739997 | 1 | I | 20160906 | 20160913 | 20160913 | PER | PHEH2016US022563 | NOVARTIS | 0.00 | F | Y | 0.00000 | 20160913 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127399971 | 12739997 | 1 | PS | RECLAST | ZOLEDRONIC ACID | 1 | Intravenous drip | UNK | 21817 | SOLUTION FOR INJECTION | |||||||||
| 127399971 | 12739997 | 2 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Unknown | UNK | U | 0 | |||||||||
| 127399971 | 12739997 | 3 | C | ATENOLOL. | ATENOLOL | 1 | Unknown | 25 MG, UNK | U | 0 | 25 | MG | |||||||
| 127399971 | 12739997 | 4 | C | CALCIUM | CALCIUM | 1 | Unknown | 500 MG, UNK | U | 0 | 500 | MG | |||||||
| 127399971 | 12739997 | 5 | C | VITAMIN D3 | CHOLECALCIFEROL | 1 | Unknown | 4000-5000 IU, UNK | U | 0 | 5000 | IU | |||||||
| 127399971 | 12739997 | 6 | C | PREDNISOLONE. | PREDNISOLONE | 1 | Unknown | 1 %, UNK | U | 0 | 1 | PCT |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127399971 | 12739997 | 1 | Product used for unknown indication |
| 127399971 | 12739997 | 2 | Product used for unknown indication |
| 127399971 | 12739997 | 3 | Product used for unknown indication |
| 127399971 | 12739997 | 4 | Product used for unknown indication |
| 127399971 | 12739997 | 5 | Product used for unknown indication |
| 127399971 | 12739997 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127399971 | 12739997 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127399971 | 12739997 | Blood pressure increased | |
| 127399971 | 12739997 | Epistaxis | |
| 127399971 | 12739997 | Eye pain | |
| 127399971 | 12739997 | Iridocyclitis | |
| 127399971 | 12739997 | Ocular hyperaemia | |
| 127399971 | 12739997 | Pain |
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 |
|---|---|---|---|---|---|---|
| 127399971 | 12739997 | 1 | 20160829 | 0 |