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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
112682694 | 11268269 | 4 | F | 20160706 | 20150714 | 20160713 | EXP | GB-DRREDDYS-GER/UKI/15/0049305 | DR REDDYS | 57.00 | YR | Y | 0.00000 | 20160713 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
112682694 | 11268269 | 1 | PS | DOCETAXEL. | DOCETAXEL | 1 | Y | U | UNKNOWN | 204193 | 60 | MG/M**2 | |||||||
112682694 | 11268269 | 2 | SS | DOCETAXEL. | DOCETAXEL | 1 | Y | U | UNKNOWN | 204193 | 75 | MG/M**2 | |||||||
112682694 | 11268269 | 3 | SS | HERCEPTIN | TRASTUZUMAB | 1 | U | 0 | |||||||||||
112682694 | 11268269 | 4 | SS | PERJETA | PERTUZUMAB | 1 | U | 0 | |||||||||||
112682694 | 11268269 | 5 | C | CYCLOPHOSPHAMIDE. | CYCLOPHOSPHAMIDE | 1 | 0 | ||||||||||||
112682694 | 11268269 | 6 | C | EPIRUBICIN | EPIRUBICIN | 1 | 0 | ||||||||||||
112682694 | 11268269 | 7 | C | FLUOROURACIL. | FLUOROURACIL | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
112682694 | 11268269 | 1 | HER-2 positive breast cancer |
112682694 | 11268269 | 3 | HER-2 positive breast cancer |
112682694 | 11268269 | 4 | HER-2 positive breast cancer |
112682694 | 11268269 | 5 | Product used for unknown indication |
112682694 | 11268269 | 6 | Product used for unknown indication |
112682694 | 11268269 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
112682694 | 11268269 | OT |
112682694 | 11268269 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
112682694 | 11268269 | Clostridium difficile infection | |
112682694 | 11268269 | Disease progression | |
112682694 | 11268269 | Lower respiratory tract infection | |
112682694 | 11268269 | Neutropenic infection | |
112682694 | 11268269 | Varicella |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |