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
126017412 12601741 2 F 2015 20160801 20160728 20160806 EXP GB-MHRA-EYC 00142533 GB-MICRO LABS LIMITED-BB2016-01090 MICRO LABS 83.00 YR M Y 97.50000 KG 20160806 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
126017412 12601741 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral U 90383
126017412 12601741 2 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral U 0
126017412 12601741 3 SS BLOOD PRESSURE MEDICATION UNSPECIFIED INGREDIENT 1 Oral U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126017412 12601741 1 Blood cholesterol increased
126017412 12601741 2 Dyspepsia
126017412 12601741 3 Preoperative care

Outcome of event

Event ID CASEID OUTC COD
126017412 12601741 LT
126017412 12601741 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126017412 12601741 Abnormal loss of weight
126017412 12601741 Amyloidosis
126017412 12601741 Arthralgia
126017412 12601741 Asthenia
126017412 12601741 Back pain
126017412 12601741 Constipation
126017412 12601741 Decreased appetite
126017412 12601741 Dysgeusia
126017412 12601741 Dyspepsia
126017412 12601741 Fatigue
126017412 12601741 Hyperproteinaemia
126017412 12601741 Hypotension
126017412 12601741 Muscle atrophy
126017412 12601741 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
126017412 12601741 1 201510 0
126017412 12601741 2 201510 0
126017412 12601741 3 2014 0