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
127757101 12775710 1 I 2016 20160915 20160923 20160923 EXP IE-AMGEN-IRLSL2016128414 AMGEN 56.00 YR A F Y 0.00000 20160923 OT IE IE

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
127757101 12775710 1 PS NEULASTA PEGFILGRASTIM 1 Subcutaneous 6 MG, AFTER CHEMO 3 1052486A 125031 6 MG UNKNOWN FORMULATION
127757101 12775710 2 C ASACOL MESALAMINE 1 Other 500 MG, QD 0 500 MG QD
127757101 12775710 3 C EMEND APREPITANT 1 Other 80 MG, QD 0 80 MG QD
127757101 12775710 4 C DEXAMETHASONE. DEXAMETHASONE 1 Other 2 MG, QD 0 2 MG QD
127757101 12775710 5 C TRAMADOL. TRAMADOL 1 Other 50 MG, QD 0 50 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127757101 12775710 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127757101 12775710 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127757101 12775710 Arthralgia
127757101 12775710 Breast operation
127757101 12775710 Breast pain
127757101 12775710 Chest pain
127757101 12775710 Dizziness
127757101 12775710 Gastrooesophageal reflux disease
127757101 12775710 Nausea
127757101 12775710 Neck pain
127757101 12775710 Nipple disorder
127757101 12775710 Pain
127757101 12775710 Stomatitis
127757101 12775710 Tinnitus
127757101 12775710 Tongue ulceration

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
127757101 12775710 1 20160831 0