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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127506182 | 12750618 | 2 | F | 20160904 | 20160913 | 20160916 | 20160926 | EXP | IT-PFIZER INC-2016430487 | PFIZER | 84.00 | YR | F | Y | 0.00000 | 20160926 | MD | IT | IT |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127506182 | 12750618 | 1 | PS | VINCRISTINE SULFATE. | VINCRISTINE SULFATE | 1 | Intravenous (not otherwise specified) | 1 DF, CYCLIC | U | 71484 | 1 | DF | |||||||
127506182 | 12750618 | 2 | SS | CYCLOPHOSPHAMIDE. | CYCLOPHOSPHAMIDE | 1 | Intravenous (not otherwise specified) | 1 DF, CYCLIC | U | 0 | 1 | DF | |||||||
127506182 | 12750618 | 3 | SS | PREDNISONE. | PREDNISONE | 1 | Intravenous (not otherwise specified) | 1 DF, CYCLIC | U | 0 | 1 | DF | |||||||
127506182 | 12750618 | 4 | SS | RITUXIMAB | RITUXIMAB | 1 | Intravenous (not otherwise specified) | 1 DF, CYCLIC | U | 0 | 1 | DF | |||||||
127506182 | 12750618 | 5 | C | RIOPAN /00141701/ | MAGALDRATE | 1 | UNK | 0 | |||||||||||
127506182 | 12750618 | 6 | C | DELTACORTENE | PREDNISONE | 1 | UNK | 0 | |||||||||||
127506182 | 12750618 | 7 | C | ALLOPURINOL. | ALLOPURINOL | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127506182 | 12750618 | 1 | B-cell lymphoma |
127506182 | 12750618 | 2 | B-cell lymphoma |
127506182 | 12750618 | 3 | B-cell lymphoma |
127506182 | 12750618 | 4 | B-cell lymphoma |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127506182 | 12750618 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127506182 | 12750618 | Diarrhoea | |
127506182 | 12750618 | Gastrointestinal disorder | |
127506182 | 12750618 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |