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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127715041 | 12771504 | 1 | I | 201508 | 20160414 | 20160922 | 20160922 | PER | US-AMGEN-USASP2016048518 | AMGEN | 36.00 | YR | A | M | Y | 0.00000 | 20160922 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127715041 | 12771504 | 1 | PS | NEUPOGEN | FILGRASTIM | 1 | Unknown | UNK | U | 103353 | SOLUTION FOR INJECTION | ||||||||
| 127715041 | 12771504 | 2 | SS | SUMATRIPTAN. | SUMATRIPTAN | 1 | Unknown | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127715041 | 12771504 | 1 | Product used for unknown indication |
| 127715041 | 12771504 | 2 | Migraine |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127715041 | 12771504 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127715041 | 12771504 | Acne | |
| 127715041 | 12771504 | Bone pain | |
| 127715041 | 12771504 | Dizziness | |
| 127715041 | 12771504 | Incorrect dose administered | |
| 127715041 | 12771504 | Migraine | |
| 127715041 | 12771504 | Neck pain | |
| 127715041 | 12771504 | Rash erythematous | |
| 127715041 | 12771504 | Spinal pain | |
| 127715041 | 12771504 | White blood cell count abnormal |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |