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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127397441 | 12739744 | 1 | I | 20160901 | 0 | 20160910 | 20160910 | DIR | FDA-CTU | 62.51 | YR | M | N | 108.00000 | KG | 20160909 | N | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127397441 | 12739744 | 1 | PS | NUVIGIL | ARMODAFINIL | 1 | 170 | 0 | 23 | MG | |||||||||
127397441 | 12739744 | 3 | C | AVASTIN | BEVACIZUMAB | 1 | 0 |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127397441 | 12739744 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127397441 | 12739744 | Blood pressure increased | |
127397441 | 12739744 | Headache | |
127397441 | 12739744 | Pulmonary embolism | |
127397441 | 12739744 | Pulmonary hypertension |
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 |
---|---|---|---|---|---|---|
127397441 | 12739744 | 1 | 20160901 | 0 |