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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124553233 | 12455323 | 3 | F | 2016 | 20160628 | 20160610 | 20160701 | EXP | GB-009507513-1604GBR010259 | MERCK | 42.00 | YR | F | Y | 0.00000 | 20160701 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124553233 | 12455323 | 1 | PS | APREPITANT. | APREPITANT | 1 | Oral | 80 MG, ONCE A DAY (TAKEN ON DAY 2 AND 3 AFTER CHEMOTHERAPY) | U | 21549 | 80 | MG | CAPSULE | QD | |||||
124553233 | 12455323 | 2 | SS | DEXAMETHASONE. | DEXAMETHASONE | 1 | Oral | 2 MG, ONCE DAILY, 3 DAYS | U | 0 | 2 | MG | TABLET | QD | |||||
124553233 | 12455323 | 3 | SS | NEULASTA | PEGFILGRASTIM | 1 | Subcutaneous | 6 MG, 24 HOURS AFTER CHEMOTHERAPY | U | 0 | 6 | MG | |||||||
124553233 | 12455323 | 4 | SS | METOCLOPRAMIDE. | METOCLOPRAMIDE | 1 | UNK | U | 0 | ||||||||||
124553233 | 12455323 | 5 | SS | LEVOMEPROMAZINE | LEVOMEPROMAZINE | 1 | UNK | U | 0 | ||||||||||
124553233 | 12455323 | 6 | SS | ONDANSETRON | ONDANSETRON | 1 | UNK | U | 0 | ||||||||||
124553233 | 12455323 | 7 | SS | cyclophosphamide (+) epirubicin hydrochloride (+) fluorouracil | CYCLOPHOSPHAMIDEEPIRUBICIN HYDROCHLORIDEFLUOROURACIL | 1 | UNK, EVERY 3 WEEKS (CYCLICAL) | U | 0 | Q3W | |||||||||
124553233 | 12455323 | 8 | SS | DOCETAXEL. | DOCETAXEL | 1 | 3 CYCLES | U | 0 |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124553233 | 12455323 | HO |
124553233 | 12455323 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124553233 | 12455323 | Arthralgia | |
124553233 | 12455323 | Constipation | |
124553233 | 12455323 | Decreased appetite | |
124553233 | 12455323 | Deep vein thrombosis | |
124553233 | 12455323 | Fatigue | |
124553233 | 12455323 | Oral pain | |
124553233 | 12455323 | Pain | |
124553233 | 12455323 | Pain in extremity | |
124553233 | 12455323 | Peripheral swelling | |
124553233 | 12455323 | Vascular pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |