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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121879566 | 12187956 | 6 | F | 20160725 | 20160317 | 20160728 | EXP | PHHY2016HU033614 | NOVARTIS | 73.00 | YR | F | Y | 58.00000 | KG | 20160728 | CN | HU | HU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121879566 | 12187956 | 1 | PS | ACLASTA | ZOLEDRONIC ACID | 1 | Intravenous (not otherwise specified) | 5 MG, UNK | 16GL0140 | 21817 | 5 | MG | SOLUTION FOR INJECTION | ||||||
| 121879566 | 12187956 | 2 | C | SYNCUMAR | ACENOCOUMAROL | 1 | Unknown | 1 DF, QD (0.5-1 MG) | 0 | 1 | DF | TABLET | QD | ||||||
| 121879566 | 12187956 | 3 | C | ALPHA D3 | 2 | Unknown | 1 UG, QD | 0 | 1 | UG | TABLET | QD | |||||||
| 121879566 | 12187956 | 4 | C | CITROKALCIUM | 2 | Unknown | 2 DF, BID | 0 | 2 | DF | TABLET | BID | |||||||
| 121879566 | 12187956 | 5 | C | MEDROL | METHYLPREDNISOLONE | 1 | Unknown | 2 DF, QD | 0 | 2 | DF | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 121879566 | 12187956 | 1 | Osteoporosis |
| 121879566 | 12187956 | 2 | Thrombosis |
| 121879566 | 12187956 | 3 | Osteoporosis |
| 121879566 | 12187956 | 4 | Osteoporosis |
| 121879566 | 12187956 | 5 | Systemic lupus erythematosus |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 121879566 | 12187956 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 121879566 | 12187956 | Abasia | |
| 121879566 | 12187956 | Bone density decreased | |
| 121879566 | 12187956 | Bone pain | |
| 121879566 | 12187956 | Dry mouth | |
| 121879566 | 12187956 | Pain | |
| 121879566 | 12187956 | Swollen tongue |
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 |
|---|---|---|---|---|---|---|
| 121879566 | 12187956 | 1 | 20151014 | 0 | ||
| 121879566 | 12187956 | 2 | 1998 | 0 | ||
| 121879566 | 12187956 | 5 | 2015 | 0 |