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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127716031 | 12771603 | 1 | I | 20160729 | 20160922 | 20160922 | PER | US-AMGEN-USASP2016099197 | AMGEN | 0.00 | F | Y | 0.00000 | 20160922 | PH | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127716031 | 12771603 | 1 | PS | NEULASTA | PEGFILGRASTIM | 1 | Unknown | UNK, DAY 1 AND DAY 8 AND DAY 15 THEN 1 WEEK OFF | U | 125031 | SOLUTION FOR INJECTION | ||||||||
127716031 | 12771603 | 2 | SS | NEUPOGEN | FILGRASTIM | 1 | Unknown | UNK, UNK | U | 0 | UNKNOWN FORMULATION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127716031 | 12771603 | 1 | Febrile neutropenia |
127716031 | 12771603 | 2 | Febrile neutropenia |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127716031 | 12771603 | Drug ineffective | |
127716031 | 12771603 | Inappropriate schedule of drug administration |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |