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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
118636687 | 11863668 | 7 | F | 20160509 | 20160624 | 20151223 | 20160701 | EXP | GB-ELI_LILLY_AND_COMPANY-GB201512004595 | ELI LILLY AND CO | 53.00 | YR | F | Y | 0.00000 | 20160701 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
118636687 | 11863668 | 1 | PS | GEMCITABINE HYDROCHLORIDE. | GEMCITABINE HYDROCHLORIDE | 1 | Unknown | UNK | U | U | 20509 | ||||||||
118636687 | 11863668 | 2 | SS | CARBOPLATIN. | CARBOPLATIN | 1 | Unknown | UNK | U | U | 0 | ||||||||
118636687 | 11863668 | 3 | SS | HERCEPTIN | TRASTUZUMAB | 1 | Subcutaneous | 600 MG, UNKNOWN | U | U | 0 | 600 | MG | ||||||
118636687 | 11863668 | 4 | SS | HERCEPTIN | TRASTUZUMAB | 1 | Subcutaneous | UNK | U | U | 0 | ||||||||
118636687 | 11863668 | 5 | SS | CHLORHEXIDINE | CHLORHEXIDINE | 1 | Unknown | U | 0 | ||||||||||
118636687 | 11863668 | 6 | C | VINORELBINE | VINORELBINEVINORELBINE TARTRATE | 1 | Oral | UNK | U | 0 | |||||||||
118636687 | 11863668 | 7 | C | GRANISETRON | GRANISETRON | 1 | UNK | U | 0 | ||||||||||
118636687 | 11863668 | 8 | C | NEULASTA | PEGFILGRASTIM | 1 | U | 0 | |||||||||||
118636687 | 11863668 | 9 | C | DEXAMETHASONE. | DEXAMETHASONE | 1 | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
118636687 | 11863668 | 1 | Product used for unknown indication |
118636687 | 11863668 | 2 | Product used for unknown indication |
118636687 | 11863668 | 3 | Product used for unknown indication |
118636687 | 11863668 | 5 | Product used for unknown indication |
118636687 | 11863668 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
118636687 | 11863668 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
118636687 | 11863668 | Allergy to chemicals | |
118636687 | 11863668 | Anaemia | |
118636687 | 11863668 | Blood creatinine increased | |
118636687 | 11863668 | Constipation | |
118636687 | 11863668 | Cough | |
118636687 | 11863668 | Dermatitis allergic | |
118636687 | 11863668 | Diarrhoea | |
118636687 | 11863668 | Dysgeusia | |
118636687 | 11863668 | Dysphonia | |
118636687 | 11863668 | Fatigue | |
118636687 | 11863668 | Hypokinesia | |
118636687 | 11863668 | Limb discomfort | |
118636687 | 11863668 | Lymphoedema | |
118636687 | 11863668 | Metastases to skin | |
118636687 | 11863668 | Musculoskeletal disorder | |
118636687 | 11863668 | Nausea | |
118636687 | 11863668 | Neuralgia | |
118636687 | 11863668 | Neuropathy peripheral | |
118636687 | 11863668 | Oedema | |
118636687 | 11863668 | Pain in extremity | |
118636687 | 11863668 | Paraesthesia | |
118636687 | 11863668 | Pruritus allergic | |
118636687 | 11863668 | Pyrexia | |
118636687 | 11863668 | Rhinorrhoea | |
118636687 | 11863668 | Sensory loss | |
118636687 | 11863668 | Vomiting | |
118636687 | 11863668 | Wound | |
118636687 | 11863668 | Wound haemorrhage | |
118636687 | 11863668 | Wound secretion |
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 |
---|---|---|---|---|---|---|
118636687 | 11863668 | 3 | 2012 | 0 |