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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125595902 | 12559590 | 2 | F | 201602 | 20160719 | 20160715 | 20160726 | EXP | PHJP2016JP019989 | NOVARTIS | 73.00 | YR | M | Y | 0.00000 | 20160726 | MD | JP | JP |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125595902 | 12559590 | 1 | PS | NEORAL | CYCLOSPORINE | 1 | Oral | 40 MG, QD | 50715 | 40 | MG | CAPSULE | QD | ||||||
125595902 | 12559590 | 2 | C | PREDONINE | PREDNISOLONEPREDNISOLONE ACETATEPREDNISOLONE SODIUM SUCCINATE | 1 | Oral | 10 MG, UNK | 0 | 10 | MG | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125595902 | 12559590 | 1 | Renal transplant |
125595902 | 12559590 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125595902 | 12559590 | OT |
125595902 | 12559590 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125595902 | 12559590 | Anaemia | |
125595902 | 12559590 | Cardiac failure | |
125595902 | 12559590 | Compression fracture | |
125595902 | 12559590 | Fall | |
125595902 | 12559590 | Fluid imbalance | |
125595902 | 12559590 | Gastric ulcer haemorrhage |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |