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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125391693 | 12539169 | 3 | F | 20160802 | 20160708 | 20160805 | EXP | GB-MHRA-ADR 23549023 | GB-009507513-1607GBR003071 | MERCK | 44.00 | YR | M | Y | 0.00000 | 20160805 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125391693 | 12539169 | 1 | PS | DEXAMETHASONE. | DEXAMETHASONE | 1 | Unknown | UNK | U | U | 12675 | TABLET | |||||||
125391693 | 12539169 | 2 | SS | ONDANSETRON HYDROCHLORIDE. | ONDANSETRON HYDROCHLORIDE | 1 | Unknown | U | U | 0 | INJECTION | ||||||||
125391693 | 12539169 | 3 | SS | AVASTIN | BEVACIZUMAB | 1 | Unknown | U | U | 0 | |||||||||
125391693 | 12539169 | 4 | SS | CARBOPLATIN. | CARBOPLATIN | 1 | Unknown | U | U | 0 | |||||||||
125391693 | 12539169 | 5 | SS | PEMETREXED DISODIUM | PEMETREXED DISODIUM | 1 | Unknown | U | U | 0 | |||||||||
125391693 | 12539169 | 6 | SS | METOCLOPRAMIDE HYDROCHLORIDE. | METOCLOPRAMIDE HYDROCHLORIDE | 1 | Unknown | U | U | 0 | |||||||||
125391693 | 12539169 | 7 | SS | NEULASTA | PEGFILGRASTIM | 1 | Unknown | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125391693 | 12539169 | 1 | Product used for unknown indication |
125391693 | 12539169 | 2 | Product used for unknown indication |
125391693 | 12539169 | 3 | Product used for unknown indication |
125391693 | 12539169 | 4 | Product used for unknown indication |
125391693 | 12539169 | 5 | Product used for unknown indication |
125391693 | 12539169 | 6 | Product used for unknown indication |
125391693 | 12539169 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125391693 | 12539169 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125391693 | 12539169 | Diarrhoea | |
125391693 | 12539169 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |