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
124403842 12440384 2 F 20160412 20160606 20160922 PER US-AMGEN-USASP2016070914 AMGEN 76.00 YR E M Y 83.90000 KG 20160922 CN 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
124403842 12440384 1 PS PROCRIT ERYTHROPOIETIN 1 Unknown UNK, Q2WK 103234 UNKNOWN FORMULATION QOW
124403842 12440384 2 SS NEUPOGEN FILGRASTIM 1 Unknown UNK, EVERY WEEK 0 UNKNOWN FORMULATION /wk
124403842 12440384 3 SS BENADRYL ALLERGY DIPHENHYDRAMINE HYDROCHLORIDE 1 Oral UNK UNK, PRN 0 TABLET
124403842 12440384 4 C PREDNISONE. PREDNISONE 1 Unknown UNK 0
124403842 12440384 5 C MULTI VITAMIN VITAMINS 1 UNK 0
124403842 12440384 6 C CALCIUM CALCIUM 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124403842 12440384 1 White blood cell count decreased
124403842 12440384 2 White blood cell count decreased
124403842 12440384 3 Rhinorrhoea
124403842 12440384 5 Supplementation therapy
124403842 12440384 6 Supplementation therapy

Outcome of event

Event ID CASEID OUTC COD
124403842 12440384 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124403842 12440384 Drug ineffective

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found