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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127274162 | 12727416 | 2 | F | 20160803 | 20160905 | 20160909 | 20160913 | EXP | PHHY2016FR122511 | SANDOZ | 60.44 | YR | M | Y | 0.00000 | 20160913 | OT | FR | FR |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127274162 | 12727416 | 1 | SS | NEORAL | CYCLOSPORINE | 1 | Oral | 400 MG, QD | 0 | 400 | MG | CAPSULE | QD | ||||||
127274162 | 12727416 | 2 | SS | SANDIMMUNE NEORAL | CYCLOSPORINE | 1 | Intravenous (not otherwise specified) | 220 MG, QD | 660 | MG | 0 | 220 | MG | SOLUTION | QD | ||||
127274162 | 12727416 | 3 | PS | BISOPROLOL | BISOPROLOL | 1 | Oral | 1 DF, QD | 75643 | 1 | DF | QD | |||||||
127274162 | 12727416 | 4 | SS | ZELITREX | VALACYCLOVIR HYDROCHLORIDE | 1 | Oral | 1 DF, QD | 8 | DF | 0 | 1 | DF | COATED TABLET | QD | ||||
127274162 | 12727416 | 5 | SS | THYMOGLOBULINE | LAPINE T-LYMPHOCYTE IMMUNE GLOBULIN | 1 | Intravenous (not otherwise specified) | UNK | 0 | ||||||||||
127274162 | 12727416 | 6 | SS | SIMVASTATINE ARROW | SIMVASTATIN | 1 | Oral | 1 DF, QD | 0 | 1 | DF | COATED TABLET | QD | ||||||
127274162 | 12727416 | 7 | SS | ZYLORIC | ALLOPURINOL | 1 | Oral | 1 DF, QD | 0 | 1 | DF | TABLET | QD | ||||||
127274162 | 12727416 | 8 | SS | TIORFAN | RACECADOTRIL | 1 | Oral | 3 DF, QD | 9 | DF | 0 | 3 | DF | CAPSULE | QD | ||||
127274162 | 12727416 | 9 | SS | DIOSMECTITE | MONTMORILLONITE | 1 | Oral | 3 DF, QD | 9 | DF | 0 | 3 | DF | QD | |||||
127274162 | 12727416 | 10 | SS | AERIUS | DESLORATADINE | 1 | Oral | 2 DF, QD | 18 | DF | 0 | 2 | DF | COATED TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127274162 | 12727416 | 1 | Product used for unknown indication |
127274162 | 12727416 | 2 | Product used for unknown indication |
127274162 | 12727416 | 3 | Product used for unknown indication |
127274162 | 12727416 | 4 | Product used for unknown indication |
127274162 | 12727416 | 5 | Product used for unknown indication |
127274162 | 12727416 | 6 | Hypercholesterolaemia |
127274162 | 12727416 | 7 | Product used for unknown indication |
127274162 | 12727416 | 8 | Product used for unknown indication |
127274162 | 12727416 | 9 | Product used for unknown indication |
127274162 | 12727416 | 10 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127274162 | 12727416 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127274162 | 12727416 | Acute kidney injury | |
127274162 | 12727416 | Confusional state | |
127274162 | 12727416 | Renal tubular necrosis | |
127274162 | 12727416 | Rhabdomyolysis | |
127274162 | 12727416 | Shock |
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 |
---|---|---|---|---|---|---|
127274162 | 12727416 | 1 | 20160812 | 20160818 | 0 | |
127274162 | 12727416 | 2 | 20160801 | 20160810 | 0 | |
127274162 | 12727416 | 3 | 20160822 | 0 | ||
127274162 | 12727416 | 4 | 20160727 | 20160822 | 0 | |
127274162 | 12727416 | 5 | 20160730 | 20160731 | 0 | |
127274162 | 12727416 | 6 | 20160821 | 0 | ||
127274162 | 12727416 | 7 | 20160818 | 0 | ||
127274162 | 12727416 | 8 | 20160801 | 20160803 | 0 | |
127274162 | 12727416 | 9 | 20160801 | 20160803 | 0 | |
127274162 | 12727416 | 10 | 20160726 | 20160803 | 0 |