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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125839641 | 12583964 | 1 | I | 20160719 | 20160722 | 20160722 | EXP | PHHY2016TR100254 | NOVARTIS | 59.00 | YR | F | Y | 0.00000 | 20160722 | CN | TR | TR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125839641 | 12583964 | 1 | PS | ACLASTA | ZOLEDRONIC ACID | 1 | Intravenous (not otherwise specified) | UNK | 21817 | ||||||||||
| 125839641 | 12583964 | 2 | C | AYRA | 2 | Oral | 16 MG, QD | U | 0 | 16 | MG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125839641 | 12583964 | 1 | Product used for unknown indication |
| 125839641 | 12583964 | 2 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125839641 | 12583964 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125839641 | 12583964 | Anger | |
| 125839641 | 12583964 | Bone pain | |
| 125839641 | 12583964 | Deafness | |
| 125839641 | 12583964 | Pain in extremity | |
| 125839641 | 12583964 | Pruritus | |
| 125839641 | 12583964 | Tension |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |