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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118708298 | 11870829 | 8 | F | 20160509 | 20160624 | 20151228 | 20160707 | EXP | GB-TEVA-618678ACC | TEVA | 53.00 | YR | F | Y | 0.00000 | 20160707 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118708298 | 11870829 | 1 | PS | CARBOPLATIN. | CARBOPLATIN | 1 | Unknown | CYCLE 10 | U | U | 77269 | ||||||||
| 118708298 | 11870829 | 2 | SS | GEMCITABINE | GEMCITABINEGEMCITABINE HYDROCHLORIDE | 1 | Unknown | CYCLE 10 | U | U | 0 | ||||||||
| 118708298 | 11870829 | 3 | SS | HERCEPTIN | TRASTUZUMAB | 1 | Subcutaneous | U | U | 0 | 600 | MG | |||||||
| 118708298 | 11870829 | 4 | SS | HERCEPTIN | TRASTUZUMAB | 1 | Subcutaneous | U | U | 0 | |||||||||
| 118708298 | 11870829 | 5 | SS | CHLORHEXIDINE | CHLORHEXIDINE | 1 | Unknown | U | U | 0 | |||||||||
| 118708298 | 11870829 | 6 | C | VINORELBINE | VINORELBINEVINORELBINE TARTRATE | 1 | Oral | 0 | |||||||||||
| 118708298 | 11870829 | 7 | C | GRANISETRON | GRANISETRON | 1 | Unknown | 0 | |||||||||||
| 118708298 | 11870829 | 8 | C | NEULASTA | PEGFILGRASTIM | 1 | Unknown | 0 | |||||||||||
| 118708298 | 11870829 | 9 | C | DEXAMETHASONE. | DEXAMETHASONE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118708298 | 11870829 | 1 | Product used for unknown indication |
| 118708298 | 11870829 | 2 | Product used for unknown indication |
| 118708298 | 11870829 | 3 | Product used for unknown indication |
| 118708298 | 11870829 | 4 | Product used for unknown indication |
| 118708298 | 11870829 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118708298 | 11870829 | HO |
| 118708298 | 11870829 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118708298 | 11870829 | Allergy to chemicals | |
| 118708298 | 11870829 | Anaemia | |
| 118708298 | 11870829 | Blood creatinine increased | |
| 118708298 | 11870829 | Breast cancer metastatic | |
| 118708298 | 11870829 | Constipation | |
| 118708298 | 11870829 | Cough | |
| 118708298 | 11870829 | Diarrhoea | |
| 118708298 | 11870829 | Dysgeusia | |
| 118708298 | 11870829 | Dysphonia | |
| 118708298 | 11870829 | Dyspnoea | |
| 118708298 | 11870829 | Fatigue | |
| 118708298 | 11870829 | Haemoglobin decreased | |
| 118708298 | 11870829 | Hyperaesthesia | |
| 118708298 | 11870829 | Hypokinesia | |
| 118708298 | 11870829 | Limb discomfort | |
| 118708298 | 11870829 | Lymphoedema | |
| 118708298 | 11870829 | Musculoskeletal disorder | |
| 118708298 | 11870829 | Nausea | |
| 118708298 | 11870829 | Neuralgia | |
| 118708298 | 11870829 | Neuropathy peripheral | |
| 118708298 | 11870829 | Oedema | |
| 118708298 | 11870829 | Pain in extremity | |
| 118708298 | 11870829 | Paraesthesia | |
| 118708298 | 11870829 | Pyrexia | |
| 118708298 | 11870829 | Rhinorrhoea | |
| 118708298 | 11870829 | Sensory loss | |
| 118708298 | 11870829 | Vomiting | |
| 118708298 | 11870829 | Wound | |
| 118708298 | 11870829 | Wound haemorrhage | |
| 118708298 | 11870829 | Wound secretion |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |