The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
127283321 12728332 1 I 2016 20160902 20160909 20160909 EXP US-AMGEN-USASP2016119436 AMGEN 70.00 YR E F Y 0.00000 20160909 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
127283321 12728332 1 PS NEULASTA PEGFILGRASTIM 1 Unknown UNK U ACM 0030 125031 SOLUTION FOR INJECTION
127283321 12728332 2 SS KEPPRA LEVETIRACETAM 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127283321 12728332 1 Product used for unknown indication
127283321 12728332 2 Brain operation

Outcome of event

Event ID CASEID OUTC COD
127283321 12728332 OT
127283321 12728332 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127283321 12728332 Adverse drug reaction
127283321 12728332 Brain operation
127283321 12728332 Cough
127283321 12728332 Fatigue
127283321 12728332 Somnolence
127283321 12728332 Throat cancer
127283321 12728332 Unevaluable event

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
127283321 12728332 2 2016 0