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
125254821 12525482 1 I 20160627 20160704 20160704 EXP US-ASTRAZENECA-2016SE70798 ASTRAZENECA 0.00 M Y 68.00000 KG 20160705 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
125254821 12525482 1 SS METOPROLOL. METOPROLOL 1 Oral 0 100 MG QD
125254821 12525482 2 PS OMEPRAZOLE. OMEPRAZOLE 1 Oral 19810 20 MG QD
125254821 12525482 3 SS BRILINTA TICAGRELOR 1 Oral 0 90 MG TABLET Q12H
125254821 12525482 4 C ACYCLOVIR. ACYCLOVIR 1 Oral 0 80 MG QD
125254821 12525482 5 C BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral 0 160.8 MG BIW
125254821 12525482 6 C TACROLIMUS. TACROLIMUS 1 Oral 0 .005 MG QD
125254821 12525482 7 C PRAVASTATIN. PRAVASTATIN 1 Oral 0 40 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125254821 12525482 3 Stent placement
125254821 12525482 4 Stem cell transplant

Outcome of event

Event ID CASEID OUTC COD
125254821 12525482 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125254821 12525482 Depression
125254821 12525482 Dyspnoea
125254821 12525482 Fatigue
125254821 12525482 Headache
125254821 12525482 Leukaemia

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
125254821 12525482 3 20160516 0