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
127587761 12758776 1 I 20110927 0 20160918 20160918 DIR US-FDA-350923 FDA-CTU 69.24 YR M N 112.50000 KG 20160918 N US US

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
127587761 12758776 1 PS ATORVASTATIN TAB ATORVASTATIN 1 N D 99 40 MG
127587761 12758776 2 SS CARVEDILOL TAB CARVEDILOL 1 0 6.25 MG COATED TABLET BID
127587761 12758776 3 SS ALLOPURINOL TAB ALLOPURINOL 1 0 100 MG COATED TABLET BID
127587761 12758776 4 SS LATANOPROST SOL. LATANOPROST 1 Ophthalmic 0 0.005 PCT
127587761 12758776 5 SS AMLODIPINE AMLODIPINE BESYLATE 1 0 5 MG
127587761 12758776 7 SS LOSARTAN TAB LOSARTAN 1 0 50 MG COATED TABLET
127587761 12758776 8 SS DYAZIDE HYDROCHLOROTHIAZIDETRIAMTERENE 1 37.25 DF 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127587761 12758776 1 Blood cholesterol increased
127587761 12758776 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127587761 12758776 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127587761 12758776 Haematocrit decreased
127587761 12758776 Haemoglobin decreased
127587761 12758776 Red blood cell count decreased
127587761 12758776 White blood cell count decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found