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
126102842 12610284 2 F 20160114 20160811 20160801 20160818 EXP DE-PFIZER INC-2016360005 PFIZER 78.00 YR M Y 96.00000 KG 20160818 MD DE DE

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
126102842 12610284 1 PS SUTENT SUNITINIB MALATE 1 37.5 MG, 2 WEEKS, ONE WEEK PAUSE (2:1) Y 21938 37.5 MG
126102842 12610284 2 SS INSUMAN RAPID INSULIN HUMAN 1 Subcutaneous UNK Y 0
126102842 12610284 3 SS LANTUS INSULIN GLARGINE 1 Subcutaneous UNK Y 0
126102842 12610284 4 C AMLODIPINE AMLODIPINE BESYLATE 1 Oral 5 MG, 1X/DAY (IN THE MORNING) 0 5 MG QD
126102842 12610284 5 C LOSARTAN. LOSARTAN 1 Oral 50 MG, DAILY 0 50 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126102842 12610284 2 Diabetes mellitus
126102842 12610284 3 Diabetes mellitus
126102842 12610284 4 Hypertension
126102842 12610284 5 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126102842 12610284 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126102842 12610284 Hyperglycaemia
126102842 12610284 Hypertensive crisis

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
126102842 12610284 1 20150915 0
126102842 12610284 2 20160115 0
126102842 12610284 3 20160115 0