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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127193401 | 12719340 | 1 | I | 2016 | 20160827 | 20160907 | 20160907 | EXP | US-AMGEN-USASP2016116412 | AMGEN | 45.00 | YR | A | F | Y | 0.00000 | 20160906 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127193401 | 12719340 | 1 | PS | NEULASTA | PEGFILGRASTIM | 1 | Unknown | UNK | U | 125031 | UNKNOWN FORMULATION | ||||||||
| 127193401 | 12719340 | 2 | C | CYTOXAN | CYCLOPHOSPHAMIDE | 1 | UNK | 0 | |||||||||||
| 127193401 | 12719340 | 3 | C | TAXOTERE | DOCETAXEL | 1 | UNK | 0 | |||||||||||
| 127193401 | 12719340 | 4 | C | TAMOXIFEN | TAMOXIFEN | 1 | UNK | 0 | |||||||||||
| 127193401 | 12719340 | 5 | C | EMEND | APREPITANT | 1 | UNK | 0 | |||||||||||
| 127193401 | 12719340 | 6 | C | ZOFRAN | ONDANSETRON HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 127193401 | 12719340 | 7 | C | ATIVAN | LORAZEPAM | 1 | UNK | 0 | |||||||||||
| 127193401 | 12719340 | 8 | C | PHENERGAN | PROMETHAZINE HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 127193401 | 12719340 | 9 | C | VITAMIN B COMPLEX | CYANOCOBALAMINDEXPANTHENOLNIACINAMIDEPYRIDOXINE HYDROCHLORIDERIBOFLAVIN 5'-PHOSPHATE SODIUMTHIAMINE HYDROCHLORIDEVITAMIN B COMPLEX | 1 | UNK | 0 | |||||||||||
| 127193401 | 12719340 | 10 | C | CLARITIN | LORATADINE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127193401 | 12719340 | 1 | Product used for unknown indication |
| 127193401 | 12719340 | 5 | Prophylaxis |
| 127193401 | 12719340 | 6 | Nausea |
| 127193401 | 12719340 | 7 | Insomnia |
| 127193401 | 12719340 | 8 | Nausea |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127193401 | 12719340 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127193401 | 12719340 | Abdominal pain upper | |
| 127193401 | 12719340 | Adverse event | |
| 127193401 | 12719340 | Back pain | |
| 127193401 | 12719340 | Diarrhoea | |
| 127193401 | 12719340 | Fatigue | |
| 127193401 | 12719340 | Feeling abnormal | |
| 127193401 | 12719340 | Full blood count decreased | |
| 127193401 | 12719340 | Hypoaesthesia oral | |
| 127193401 | 12719340 | Laziness | |
| 127193401 | 12719340 | Muscular weakness | |
| 127193401 | 12719340 | Nausea | |
| 127193401 | 12719340 | Nightmare | |
| 127193401 | 12719340 | Paraesthesia | |
| 127193401 | 12719340 | Poor quality sleep | |
| 127193401 | 12719340 | Pyrexia | |
| 127193401 | 12719340 | Scar | |
| 127193401 | 12719340 | Tachycardia | |
| 127193401 | 12719340 | Tooth disorder | |
| 127193401 | 12719340 | Toothache | |
| 127193401 | 12719340 | Uterine disorder | |
| 127193401 | 12719340 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 127193401 | 12719340 | 1 | 2016 | 0 | ||
| 127193401 | 12719340 | 2 | 20160722 | 0 | ||
| 127193401 | 12719340 | 3 | 20160722 | 0 | ||
| 127193401 | 12719340 | 5 | 2016 | 0 | ||
| 127193401 | 12719340 | 6 | 2016 | 0 | ||
| 127193401 | 12719340 | 7 | 2016 | 0 | ||
| 127193401 | 12719340 | 8 | 2016 | 0 | ||
| 127193401 | 12719340 | 10 | 2016 | 0 |