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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124983282 | 12498328 | 2 | F | 20160707 | 20160627 | 20160721 | EXP | GB-CIPLA LTD.-2016GB07443 | CIPLA | 0.00 | Y | 0.00000 | 20160721 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124983282 | 12498328 | 1 | PS | CARBOPLATIN. | CARBOPLATIN | 1 | Unknown | UNK | U | U | 77383 | ||||||||
124983282 | 12498328 | 2 | SS | GEMCITABINE | GEMCITABINEGEMCITABINE HYDROCHLORIDE | 1 | Intravenous (not otherwise specified) | UNK | U | U | 0 | ||||||||
124983282 | 12498328 | 3 | SS | CAPECITABINE. | CAPECITABINE | 1 | Unknown | UNKNOWN | U | U | 0 | ||||||||
124983282 | 12498328 | 4 | SS | VINORELBINE | VINORELBINEVINORELBINE TARTRATE | 1 | Unknown | UNK | U | U | 0 | ||||||||
124983282 | 12498328 | 5 | SS | HERCEPTIN | TRASTUZUMAB | 1 | Subcutaneous | 600 MG, UNK | U | U | 0 | 600 | MG | ||||||
124983282 | 12498328 | 6 | C | HEPARIN | HEPARIN SODIUM | 1 | Intravenous (not otherwise specified) | UNK | U | U | 0 | ||||||||
124983282 | 12498328 | 7 | C | Ondansetron | ONDANSETRON | 1 | Oral | 8 MG, UNK | U | U | 0 | 8 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124983282 | 12498328 | 1 | Product used for unknown indication |
124983282 | 12498328 | 2 | Product used for unknown indication |
124983282 | 12498328 | 3 | Product used for unknown indication |
124983282 | 12498328 | 4 | Product used for unknown indication |
124983282 | 12498328 | 5 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124983282 | 12498328 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124983282 | 12498328 | Constipation | |
124983282 | 12498328 | Cough | |
124983282 | 12498328 | Diarrhoea | |
124983282 | 12498328 | Dyspnoea exertional | |
124983282 | 12498328 | Fatigue | |
124983282 | 12498328 | Haemoglobin abnormal | |
124983282 | 12498328 | Herpes zoster | |
124983282 | 12498328 | Infected skin ulcer | |
124983282 | 12498328 | Lethargy | |
124983282 | 12498328 | Malaise | |
124983282 | 12498328 | Musculoskeletal stiffness | |
124983282 | 12498328 | Nausea | |
124983282 | 12498328 | Neutropenia | |
124983282 | 12498328 | Neutrophil count abnormal | |
124983282 | 12498328 | Poor quality sleep | |
124983282 | 12498328 | Rash | |
124983282 | 12498328 | Tachycardia | |
124983282 | 12498328 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |