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
127273031 12727303 1 I 20091123 20160826 20160909 20160909 EXP 372346 IT-ACCORD-043745 ACCORD 48.00 YR F Y 0.00000 20160909 MD IT IT

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
127273031 12727303 1 PS SIMVASTATIN. SIMVASTATIN 1 Y U 78155
127273031 12727303 2 SS PRAVASTATIN. PRAVASTATIN 1 Y U 2147483647
127273031 12727303 3 SS ATORVASTATIN/ATORVASTATIN CALCIUM ATORVASTATIN CALCIUM 1 Y U 0
127273031 12727303 4 SS ROSUVASTATIN/ROSUVASTATIN CALCIUM ROSUVASTATIN CALCIUM 1 Y U 0
127273031 12727303 5 C LEVOTHYROXINE/LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM 1 0
127273031 12727303 6 C OLMESARTAN OLMESARTAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127273031 12727303 1 Type IIa hyperlipidaemia
127273031 12727303 2 Type IIa hyperlipidaemia
127273031 12727303 3 Type IIa hyperlipidaemia
127273031 12727303 4 Type IIa hyperlipidaemia
127273031 12727303 5 Product used for unknown indication
127273031 12727303 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127273031 12727303 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127273031 12727303 Asthenia
127273031 12727303 Myopathy Myopathy
127273031 12727303 Pain in extremity Pain in extremity

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found