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
126049871 12604987 1 I 2015 20160725 20160728 20160728 EXP GB-ASTRAZENECA-2016SE80575 ASTRAZENECA 83.00 YR M Y 97.50000 KG 20160729 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
126049871 12604987 1 PS OMEPRAZOLE. OMEPRAZOLE 1 Oral 19810
126049871 12604987 2 SS SIMVASTATIN. SIMVASTATIN 1 Oral 0
126049871 12604987 3 SS BLOOD PRESSURE MEDICATION UNSPECIFIED INGREDIENT 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126049871 12604987 1 Dyspepsia
126049871 12604987 2 Blood cholesterol increased
126049871 12604987 3 Preoperative care

Outcome of event

Event ID CASEID OUTC COD
126049871 12604987 LT
126049871 12604987 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126049871 12604987 Abnormal loss of weight
126049871 12604987 Amyloidosis
126049871 12604987 Arthralgia
126049871 12604987 Asthenia
126049871 12604987 Back pain
126049871 12604987 Constipation
126049871 12604987 Decreased appetite
126049871 12604987 Dysgeusia
126049871 12604987 Dyspepsia
126049871 12604987 Fatigue
126049871 12604987 Hyperproteinaemia
126049871 12604987 Hypotension
126049871 12604987 Muscle atrophy
126049871 12604987 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
126049871 12604987 1 201510 0
126049871 12604987 2 201510 0
126049871 12604987 3 2014 0