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
127251541 12725154 1 I 20130909 0 20160905 20160905 DIR US-FDA-349824 FDA-CTU 69.00 YR F N 59.40000 KG 20160905 N 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
127251541 12725154 1 PS SIMVASTATIN ACCORD HEA SIMVASTATIN 1 Oral Y Y 20170314 0 90 DF COATED TABLET HS
127251541 12725154 2 SS LIPITOR ATORVASTATIN CALCIUM 1 Oral Y Y 0 HS
127251541 12725154 4 C HRT UNSPECIFIED INGREDIENT 1 0
127251541 12725154 6 C LOSARTAN. LOSARTAN 1 0
127251541 12725154 8 C FISH OIL FISH OIL 1 0
127251541 12725154 10 C VITAMIN D CHOLECALCIFEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127251541 12725154 1 Blood cholesterol increased
127251541 12725154 2 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
127251541 12725154 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127251541 12725154 Activities of daily living impaired
127251541 12725154 Blood glucose abnormal
127251541 12725154 Cough
127251541 12725154 Fatigue
127251541 12725154 Hypertension
127251541 12725154 Nephrolithiasis
127251541 12725154 Rash

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
127251541 12725154 1 20150107 20160518 0
127251541 12725154 2 20100304 20130514 0