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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124666852 | 12466685 | 2 | F | 20160802 | 20160615 | 20160812 | EXP | GB-BAUSCH-BL-2016-013818 | BAUSCH AND LOMB | 52.00 | YR | M | Y | 0.00000 | 20160812 | MD | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124666852 | 12466685 | 1 | PS | PREDNISOLONE. | PREDNISOLONE | 1 | Unknown | U | 40070 | 5 | MG | TABLET | |||||||
124666852 | 12466685 | 2 | SS | AZATHIOPRINE. | AZATHIOPRINE | 1 | Unknown | U | 0 | 50 | MG | ||||||||
124666852 | 12466685 | 3 | SS | AZATHIOPRINE. | AZATHIOPRINE | 1 | Unknown | U | 0 | 25 | MG | ||||||||
124666852 | 12466685 | 4 | SS | ADOPORT | TACROLIMUS | 1 | Unknown | U | 0 | 1 | MG | CAPSULE | |||||||
124666852 | 12466685 | 5 | SS | ADOPORT | TACROLIMUS | 1 | Unknown | U | 0 | .5 | MG | CAPSULE |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124666852 | 12466685 | 1 | Immunosuppression |
124666852 | 12466685 | 2 | Immunosuppression |
124666852 | 12466685 | 4 | Immunosuppression |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124666852 | 12466685 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124666852 | 12466685 | Abdominal pain | |
124666852 | 12466685 | Malaise |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |