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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123141123 | 12314112 | 3 | F | 20151106 | 20160628 | 20160428 | 20160701 | EXP | GB-MHRA-ADR 23439617 | GB-WEST-WARD PHARMACEUTICALS CORP.-GB-H14001-16-00645 | WESTWARD | 58.00 | YR | F | Y | 0.00000 | 20160630 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123141123 | 12314112 | 1 | PS | CIPROFLOXACIN. | CIPROFLOXACIN | 1 | Unknown | 76558 | |||||||||||
| 123141123 | 12314112 | 2 | SS | AVASTIN | BEVACIZUMAB | 1 | Unknown | 0 | |||||||||||
| 123141123 | 12314112 | 3 | SS | CAPECITABINE. | CAPECITABINE | 1 | Unknown | 0 | |||||||||||
| 123141123 | 12314112 | 4 | SS | PACLITAXEL. | PACLITAXEL | 1 | Unknown | 0 | |||||||||||
| 123141123 | 12314112 | 5 | SS | ZOMETA | ZOLEDRONIC ACID | 1 | Unknown | 0 | |||||||||||
| 123141123 | 12314112 | 6 | SS | ZOMETA | ZOLEDRONIC ACID | 1 | Unknown | 0 | |||||||||||
| 123141123 | 12314112 | 7 | SS | ZOMETA | ZOLEDRONIC ACID | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123141123 | 12314112 | 1 | Product used for unknown indication |
| 123141123 | 12314112 | 2 | Product used for unknown indication |
| 123141123 | 12314112 | 3 | Product used for unknown indication |
| 123141123 | 12314112 | 4 | Product used for unknown indication |
| 123141123 | 12314112 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123141123 | 12314112 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123141123 | 12314112 | Alopecia | |
| 123141123 | 12314112 | Decreased appetite | |
| 123141123 | 12314112 | Device related infection | |
| 123141123 | 12314112 | Diarrhoea | |
| 123141123 | 12314112 | Dyspnoea | |
| 123141123 | 12314112 | Fatigue | |
| 123141123 | 12314112 | Lethargy | |
| 123141123 | 12314112 | Malaise | |
| 123141123 | 12314112 | Neuropathy peripheral | |
| 123141123 | 12314112 | Pleural effusion | |
| 123141123 | 12314112 | Pneumonia | |
| 123141123 | 12314112 | Pulmonary oedema |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |