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
125782661 12578266 1 I 20131201 20160718 20160721 20160721 EXP GB-MHRA-EYC 00142377 GB-MICRO LABS LIMITED-BB2016-01047 MICRO LABS 72.00 YR F Y 66.67000 KG 20160721 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
125782661 12578266 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral N U 90383 20 MG
125782661 12578266 2 SS SIMVASTATIN. SIMVASTATIN 1 Oral N U 90383 40 MG
125782661 12578266 3 C INDERAL LA PROPRANOLOL HYDROCHLORIDE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125782661 12578266 1 Type IIa hyperlipidaemia
125782661 12578266 2 Type IIa hyperlipidaemia
125782661 12578266 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125782661 12578266 HO
125782661 12578266 DS
125782661 12578266 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125782661 12578266 Motor dysfunction
125782661 12578266 Muscle spasms
125782661 12578266 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
125782661 12578266 1 20130801 201309 0
125782661 12578266 2 20140101 0