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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121887097 | 12188709 | 7 | F | 20160127 | 20160701 | 20160317 | 20160712 | EXP | GB-ACTAVIS-2016-05873 | WATSON | 30.00 | YR | F | Y | 0.00000 | 20160712 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121887097 | 12188709 | 1 | SS | Epirubicin (Unknown) | EPIRUBICIN | 1 | Unknown | UNK | U | UNCONFIRMED | 0 | UNK | |||||||
121887097 | 12188709 | 2 | PS | Dexamethasone (Unknown) | DEXAMETHASONE | 1 | Unknown | UNK, UNKNOWN | U | UNCONFIRMED | 85456 | UNK | |||||||
121887097 | 12188709 | 3 | SS | Metoclopramide (Unknown) | METOCLOPRAMIDE | 1 | Unknown | UNK, UNKNOWN | U | UNCONFIRMED | 0 | UNK | |||||||
121887097 | 12188709 | 4 | SS | Ondansetron (Unknown) | ONDANSETRON | 1 | Unknown | UNK, UNKNOWN | U | UNCONFIRMED | 0 | UNK | |||||||
121887097 | 12188709 | 5 | SS | NEULASTA | PEGFILGRASTIM | 1 | Unknown | UNK, CYCLE 2 DAY 9, (CYCLICAL) | U | 0 | |||||||||
121887097 | 12188709 | 6 | SS | ZOMETA | ZOLEDRONIC ACID | 1 | Unknown | UNK | U | 0 | |||||||||
121887097 | 12188709 | 7 | SS | APREPITANT. | APREPITANT | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
121887097 | 12188709 | 8 | SS | CALCICHEW D3 | CALCIUMCHOLECALCIFEROL | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
121887097 | 12188709 | 9 | SS | LEVOMEPROMAZINE | LEVOMEPROMAZINE | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
121887097 | 12188709 | 10 | SS | TAXOTERE | DOCETAXEL | 1 | Unknown | UNK, UNKNOWN | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
121887097 | 12188709 | 1 | Product used for unknown indication |
121887097 | 12188709 | 2 | Product used for unknown indication |
121887097 | 12188709 | 3 | Product used for unknown indication |
121887097 | 12188709 | 4 | Product used for unknown indication |
121887097 | 12188709 | 5 | Product used for unknown indication |
121887097 | 12188709 | 6 | Product used for unknown indication |
121887097 | 12188709 | 7 | Product used for unknown indication |
121887097 | 12188709 | 8 | Product used for unknown indication |
121887097 | 12188709 | 9 | Product used for unknown indication |
121887097 | 12188709 | 10 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
121887097 | 12188709 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
121887097 | 12188709 | Alopecia | |
121887097 | 12188709 | Back pain | |
121887097 | 12188709 | Constipation | |
121887097 | 12188709 | Dysgeusia | |
121887097 | 12188709 | Fatigue | |
121887097 | 12188709 | Neuropathy peripheral | |
121887097 | 12188709 | Paraesthesia oral | |
121887097 | 12188709 | Phlebitis | |
121887097 | 12188709 | Skin discolouration | |
121887097 | 12188709 | Sunburn |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |