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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1061378818 | 10613788 | 18 | F | 20141124 | 20160629 | 20141128 | 20160701 | EXP | CN-009507513-1411CHN012400 | MERCK | 54.00 | YR | M | Y | 59.70000 | KG | 20160701 | MD | CN | CN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1061378818 | 10613788 | 1 | PS | EMEND | APREPITANT | 1 | Oral | 125 MG, ONCE, DAY 1 | 205 | MG | Y1248 | 21549 | 125 | MG | CAPSULE | 1X | |||
1061378818 | 10613788 | 2 | SS | EMEND | APREPITANT | 1 | Oral | 80 MG, QD, DAY 2 AND DAY 3 | 205 | MG | Y1248 | 21549 | 80 | MG | CAPSULE | QD | |||
1061378818 | 10613788 | 3 | SS | CISPLATIN. | CISPLATIN | 1 | Intravenous drip | 40 MG, QD, DAY 1 TO 3; TREATMENT REGIMEN CIS-PLATINUM COMPLEXES + ETOPOSIDE | 120 | MG | 0 | 40 | MG | INJECTION | QD | ||||
1061378818 | 10613788 | 4 | SS | ETOPOSIDE. | ETOPOSIDE | 1 | Intravenous drip | 200 MG, QD, DAY 1 TO 3; TREATMENT REGIMEN CIS-PLATINUM COMPLEXES + ETOPOSIDE | 600 | MG | 0 | 200 | MG | INJECTION | QD | ||||
1061378818 | 10613788 | 5 | C | GLUTATHIONE | GLUTATHIONE | 1 | Intravenous drip | 1.8 G, QD | 5.4000001 | G | U | 0 | 1.8 | G | INJECTION | QD | |||
1061378818 | 10613788 | 6 | C | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Intravenous drip | 42.3 MG, QD | 126.900002 | MG | U | 0 | 42.3 | MG | INJECTION | QD | |||
1061378818 | 10613788 | 7 | C | SODIUM BICARBONATE. | SODIUM BICARBONATE | 1 | Intravenous drip | 50ML/CC DAILY, STRENGTH 5% *1ML | 150 | ML | U | 0 | 50 | ML | INJECTION | QD | |||
1061378818 | 10613788 | 8 | C | calcium gluconate (+) magnesium sulfate (+) potassium chloride (+) sod | 2 | Intravenous drip | TOTAL DAILY DOSE 500 ML/CC | 1500 | ML | U | 0 | 500 | ML | INJECTION | QD | ||||
1061378818 | 10613788 | 9 | C | ONDANSETRON | ONDANSETRON | 1 | Intravenous (not otherwise specified) | 8 MG, QD, STRENGTH 4MG/2ML | 16 | MG | U | 0 | 8 | MG | INJECTION | QD | |||
1061378818 | 10613788 | 10 | C | DEXAMETHASONE. | DEXAMETHASONE | 1 | Oral | 12 MG, QD | 24 | MG | U | 0 | 12 | MG | TABLET | QD | |||
1061378818 | 10613788 | 11 | C | MANNITOL. | MANNITOL | 1 | Intravenous drip | 50 G, QD, 50G/250ML | 150 | G | U | 0 | 50 | G | INJECTION | QD | |||
1061378818 | 10613788 | 12 | C | ENOXAPARIN SODIUM. | ENOXAPARIN SODIUM | 1 | Subcutaneous | 80 MG, QD | 240 | MG | U | 0 | 80 | MG | INJECTION | QD | |||
1061378818 | 10613788 | 13 | C | ZOLEDRONIC ACID | ZOLEDRONIC ACID | 1 | Intravenous drip | 4 MG, QD | 4 | MG | U | 0 | 4 | MG | INJECTION | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
1061378818 | 10613788 | 1 | Prophylaxis of nausea and vomiting |
1061378818 | 10613788 | 3 | Chemotherapy |
1061378818 | 10613788 | 4 | Chemotherapy |
1061378818 | 10613788 | 5 | Prophylaxis |
1061378818 | 10613788 | 6 | Prophylaxis |
1061378818 | 10613788 | 7 | Urine abnormality |
1061378818 | 10613788 | 8 | Electrolyte substitution therapy |
1061378818 | 10613788 | 9 | Vomiting |
1061378818 | 10613788 | 10 | Vomiting |
1061378818 | 10613788 | 11 | Polyuria |
1061378818 | 10613788 | 12 | Thrombosis prophylaxis |
1061378818 | 10613788 | 13 | Prophylaxis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
1061378818 | 10613788 | HO |
1061378818 | 10613788 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
1061378818 | 10613788 | Bone marrow failure | |
1061378818 | 10613788 | Febrile neutropenia | |
1061378818 | 10613788 | Hypocalcaemia | |
1061378818 | 10613788 | Hypokalaemia | |
1061378818 | 10613788 | Hyponatraemia | |
1061378818 | 10613788 | Neuralgia |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
1061378818 | 10613788 | 1 | 20141113 | 20141113 | 0 | |
1061378818 | 10613788 | 2 | 20141114 | 20141115 | 0 | |
1061378818 | 10613788 | 3 | 20141113 | 20141115 | 0 | |
1061378818 | 10613788 | 4 | 20141113 | 20141115 | 0 | |
1061378818 | 10613788 | 5 | 20141113 | 20141115 | 0 | |
1061378818 | 10613788 | 6 | 20141113 | 20141115 | 0 | |
1061378818 | 10613788 | 7 | 20141113 | 20141115 | 0 | |
1061378818 | 10613788 | 8 | 20141113 | 20141115 | 0 | |
1061378818 | 10613788 | 9 | 20141113 | 20141115 | 0 | |
1061378818 | 10613788 | 10 | 20141113 | 20141115 | 0 | |
1061378818 | 10613788 | 11 | 20141113 | 20141115 | 0 | |
1061378818 | 10613788 | 12 | 20141114 | 20141116 | 0 | |
1061378818 | 10613788 | 13 | 20141116 | 20141116 | 0 |