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
126122362 12612236 2 F 2015 20160801 20160801 20160803 EXP GB-MHRA-EYC 00142533 GB-009507513-1607GBR012864 MERCK 83.00 YR M Y 97.50000 KG 20160803 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
126122362 12612236 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral UNK U 19766 TABLET
126122362 12612236 2 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral UNK U 0 CAPSULE
126122362 12612236 3 SS OMEPRAZOLE. OMEPRAZOLE 1 U 0 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126122362 12612236 1 Blood cholesterol increased
126122362 12612236 2 Dyspepsia
126122362 12612236 3 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
126122362 12612236 DS
126122362 12612236 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126122362 12612236 Abnormal loss of weight
126122362 12612236 Amyloidosis
126122362 12612236 Arthralgia
126122362 12612236 Asthenia
126122362 12612236 Back pain
126122362 12612236 Constipation
126122362 12612236 Decreased appetite
126122362 12612236 Dysgeusia
126122362 12612236 Dyspepsia
126122362 12612236 Fatigue
126122362 12612236 Hyperproteinaemia
126122362 12612236 Hypotension
126122362 12612236 Muscle atrophy
126122362 12612236 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
126122362 12612236 1 201510 0
126122362 12612236 2 201510 0