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
126287711 12628771 1 I 2015 20160725 20160808 20160808 EXP GB-MHRA-EYC 00142533 GB-LUPIN PHARMACEUTICALS INC.-E2B_00005927 LUPIN 83.00 YR M Y 97.52000 KG 20160808 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
126287711 12628771 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral U UNKNOWN 78103
126287711 12628771 2 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral U UNKNOWN 202384

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126287711 12628771 1 Blood cholesterol increased
126287711 12628771 2 Dyspepsia

Outcome of event

Event ID CASEID OUTC COD
126287711 12628771 DS
126287711 12628771 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126287711 12628771 Abnormal loss of weight
126287711 12628771 Amyloidosis
126287711 12628771 Arthralgia
126287711 12628771 Asthenia
126287711 12628771 Back pain
126287711 12628771 Constipation
126287711 12628771 Decreased appetite
126287711 12628771 Dysgeusia
126287711 12628771 Dyspepsia
126287711 12628771 Fatigue
126287711 12628771 Hyperproteinaemia
126287711 12628771 Hypotension
126287711 12628771 Muscle atrophy
126287711 12628771 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
126287711 12628771 1 201510 0
126287711 12628771 2 201510 0