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
126044701 12604470 1 I 20131201 20160718 20160728 20160728 EXP GB-MHRA-EYC 00142377 GB-MYLANLABS-2016M1029853 MYLAN 0.00 Y 0.00000 20160728 CN GB GB

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
126044701 12604470 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral 20 MG, UNK N U 90868 20 MG
126044701 12604470 2 SS SIMVASTATIN. SIMVASTATIN 1 Oral 40 MG, UNK N U 90868 40 MG
126044701 12604470 3 C INDERAL PROPRANOLOL HYDROCHLORIDE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126044701 12604470 1 Type IIa hyperlipidaemia

Outcome of event

Event ID CASEID OUTC COD
126044701 12604470 OT
126044701 12604470 HO
126044701 12604470 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126044701 12604470 Motor dysfunction
126044701 12604470 Muscle spasms
126044701 12604470 Myalgia

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
126044701 12604470 1 20130801 201309 0
126044701 12604470 2 20140101 0