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
126257492 12625749 2 F 2015 20160801 20160805 20160811 EXP GB-MHRA-EYC 00142533 GB-TEVA-681012ACC TEVA 83.00 YR M Y 97.52000 KG 20160811 MD 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
126257492 12625749 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral U 76052
126257492 12625749 2 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126257492 12625749 1 Blood cholesterol increased
126257492 12625749 2 Dyspepsia

Outcome of event

Event ID CASEID OUTC COD
126257492 12625749 DS
126257492 12625749 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126257492 12625749 Abnormal loss of weight
126257492 12625749 Amyloidosis
126257492 12625749 Arthralgia
126257492 12625749 Asthenia
126257492 12625749 Back pain
126257492 12625749 Constipation
126257492 12625749 Decreased appetite
126257492 12625749 Dysgeusia
126257492 12625749 Dyspepsia
126257492 12625749 Fatigue
126257492 12625749 Hyperproteinaemia
126257492 12625749 Hypotension
126257492 12625749 Muscle atrophy
126257492 12625749 Muscle spasms

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
126257492 12625749 1 201510 0
126257492 12625749 2 201510 0