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
126214552 12621455 2 F 2015 20160801 20160804 20160804 EXP GB-MHRA-EYC 00142533 GB-DRREDDYS-GER/UKI/16/0081869 DR REDDYS 83.00 YR M Y 97.52000 KG 20160804 MD 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
126214552 12621455 1 PS OMEPRAZOLE. OMEPRAZOLE 1 Oral U UNKNOWN 75576
126214552 12621455 2 SS SIMVASTATIN. SIMVASTATIN 1 Oral U 0
126214552 12621455 3 SS BLOOD PRESSURE MEDICATION UNSPECIFIED INGREDIENT 1 Oral U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126214552 12621455 1 Dyspepsia
126214552 12621455 2 Blood cholesterol increased
126214552 12621455 3 Preoperative care

Outcome of event

Event ID CASEID OUTC COD
126214552 12621455 LT
126214552 12621455 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126214552 12621455 Abnormal loss of weight
126214552 12621455 Amyloidosis
126214552 12621455 Arthralgia
126214552 12621455 Asthenia
126214552 12621455 Back pain
126214552 12621455 Constipation
126214552 12621455 Decreased appetite
126214552 12621455 Dysgeusia
126214552 12621455 Dyspepsia
126214552 12621455 Fatigue
126214552 12621455 Hyperproteinaemia
126214552 12621455 Hypotension
126214552 12621455 Muscle atrophy
126214552 12621455 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
126214552 12621455 1 201510 0
126214552 12621455 2 201510 0
126214552 12621455 3 2014 0