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
126824702 12682470 2 F 20160511 20160829 20160825 20160831 EXP US-AMGEN-USASP2016108876 AMGEN 60.00 YR A M Y 82.54000 KG 20160831 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
126824702 12682470 1 PS PROCRIT ERYTHROPOIETIN 1 Intravenous (not otherwise specified) 40,000 UNITS, WHEN HE NEEDS IT U 103234 SOLUTION FOR INJECTION
126824702 12682470 2 C ACYCLOVIR. ACYCLOVIR 1 UNK 0
126824702 12682470 3 C ESCITALOPRAM ESCITALOPRAM OXALATE 1 UNK 0
126824702 12682470 4 C CALCIUM/VITAMIN D CALCIUMVITAMIN D 1 UNK 0
126824702 12682470 5 C DEXTROMETHORPHAN DEXTROMETHORPHAN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126824702 12682470 1 Anaemia

Outcome of event

Event ID CASEID OUTC COD
126824702 12682470 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126824702 12682470 Drug ineffective
126824702 12682470 Haemoglobin abnormal
126824702 12682470 Transfusion

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
126824702 12682470 1 20140217 20160511 0