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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127616321 | 12761632 | 1 | I | 20160525 | 20160907 | 20160920 | 20160920 | EXP | GB-BAUSCH-BL-2016-022040 | BAUSCH AND LOMB | 48.00 | YR | M | Y | 70.00000 | KG | 20160920 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127616321 | 12761632 | 1 | PS | PREDNISOLONE. | PREDNISOLONE | 1 | Unknown | 40070 | 10 | MG | QD | ||||||||
127616321 | 12761632 | 2 | SS | PREDNISOLONE. | PREDNISOLONE | 1 | Unknown | 40070 | 20 | MG | QD | ||||||||
127616321 | 12761632 | 3 | SS | ETANERCEPT | ETANERCEPT | 1 | Intradermal | D | 0 | 1 | MG | /wk | |||||||
127616321 | 12761632 | 4 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Subcutaneous | U | 0 | 25 | MG | /wk | |||||||
127616321 | 12761632 | 5 | C | FOLIC ACID. | FOLIC ACID | 1 | 0 | ||||||||||||
127616321 | 12761632 | 6 | C | ORAMORPH | MORPHINE SULFATE | 1 | 0 | ||||||||||||
127616321 | 12761632 | 7 | C | VOLTAROL | DICLOFENAC SODIUM | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127616321 | 12761632 | 1 | Product used for unknown indication |
127616321 | 12761632 | 3 | Product used for unknown indication |
127616321 | 12761632 | 4 | Product used for unknown indication |
127616321 | 12761632 | 5 | Product used for unknown indication |
127616321 | 12761632 | 6 | Product used for unknown indication |
127616321 | 12761632 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127616321 | 12761632 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127616321 | 12761632 | Sepsis |
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 |
---|---|---|---|---|---|---|
127616321 | 12761632 | 1 | 20151220 | 0 | ||
127616321 | 12761632 | 3 | 20160215 | 20160510 | 0 | |
127616321 | 12761632 | 4 | 20131001 | 0 | ||
127616321 | 12761632 | 5 | 20131001 | 0 | ||
127616321 | 12761632 | 6 | 20160521 | 0 | ||
127616321 | 12761632 | 7 | 20160521 | 20160523 | 0 |