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
126482831 12648283 1 I 20160731 20160805 20160812 20160812 EXP DE-SA-2016SA145521 AVENTIS 76.00 YR E M Y 85.00000 KG 20160812 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
126482831 12648283 1 PS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 Oral U 20839 75 MG QD
126482831 12648283 2 SS MARCUMAR PHENPROCOUMON 1 Oral U 0 3 MG QD
126482831 12648283 3 SS ASPIRIN. ASPIRIN 1 Oral U 0 100 MG QD
126482831 12648283 4 C PANTOZOL PANTOPRAZOLE SODIUM 1 Oral 0 40 MG QD
126482831 12648283 5 C SIMVASTATIN. SIMVASTATIN 1 Oral 0 40 MG QD
126482831 12648283 6 C RAMIPRIL. RAMIPRIL 1 Oral 0 2.5 MG QD
126482831 12648283 7 C L-THYROXIN LEVOTHYROXINE SODIUM 1 Oral 0 25 UG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126482831 12648283 4 Prophylaxis
126482831 12648283 5 Hypercholesterolaemia
126482831 12648283 6 Hypertension
126482831 12648283 7 Hyperthyroidism

Outcome of event

Event ID CASEID OUTC COD
126482831 12648283 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126482831 12648283 Anxiety
126482831 12648283 Hypertension
126482831 12648283 Nervousness

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
126482831 12648283 1 20160722 20160731 0
126482831 12648283 2 20160726 20160731 0
126482831 12648283 3 20160722 20160731 0
126482831 12648283 4 20160722 20160731 0
126482831 12648283 5 20160722 20160731 0
126482831 12648283 6 20160722 20160731 0
126482831 12648283 7 1996 20160731 0