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
126109672 12610967 2 F 2015 20160801 20160801 20160809 EXP GB-MHRA-EYC 00142533 PHHY2016GB102352 SANDOZ 83.00 YR M Y 97.50000 KG 20160809 OT 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
126109672 12610967 1 PS OMEPRAZOLE. OMEPRAZOLE 1 Oral 75757
126109672 12610967 2 SS SIMVASTATIN. SIMVASTATIN 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126109672 12610967 1 Dyspepsia
126109672 12610967 2 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
126109672 12610967 DS
126109672 12610967 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126109672 12610967 Abnormal loss of weight
126109672 12610967 Amyloidosis
126109672 12610967 Arthralgia
126109672 12610967 Asthenia
126109672 12610967 Back pain
126109672 12610967 Constipation
126109672 12610967 Decreased appetite
126109672 12610967 Dysgeusia
126109672 12610967 Dyspepsia
126109672 12610967 Fatigue
126109672 12610967 Hyperproteinaemia
126109672 12610967 Hypotension
126109672 12610967 Muscle atrophy
126109672 12610967 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
126109672 12610967 1 201510 0
126109672 12610967 2 201510 0