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
70683502 7068350 2 F 20090211 20131218 20090724 20131231 EXP 2009S1005558 CB FLEET 68.00 YR M N 0.00000 20131230 LW 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
70683502 7068350 1 PS FLEET PHOSPHO-SODA 1 ORAL 2 IN 24 HOURS D D 0 90 ML
70683502 7068350 3 C ATACAND (CANDESARTAN CILEXETIL) 2 0
70683502 7068350 5 C LASIX (FUROSEMIDE) 1 0
70683502 7068350 7 C ATENOLOL (ATENOLOL) 1 0
70683502 7068350 9 C ALLOPURINOL (ALLOPURINOL) 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
70683502 7068350 1 Colonoscopy

Outcome of event

Event ID CASEID OUTC COD
70683502 7068350 OT
70683502 7068350 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
70683502 7068350 Asthenia
70683502 7068350 Haemorrhoids
70683502 7068350 Hypotension
70683502 7068350 Kidney enlargement
70683502 7068350 Renal failure chronic

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

Event ID CASEID RPSR COD
70683502 7068350 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
70683502 7068350 1 20080306 20080306 0