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
125798331 12579833 1 I 201209 20160714 20160721 20160721 EXP GR-GREOF-20160185 GR-PFIZER INC-2016348999 PFIZER 62.00 YR M Y 118.00000 KG 20160721 MD GR GR

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
125798331 12579833 1 PS LIPITOR ATORVASTATIN CALCIUM 1 Oral 10 MG, 1X/DAY Y 20702 10 MG QD
125798331 12579833 2 C GLUCOPHAGE METFORMIN HYDROCHLORIDE 1 Oral 1000 MG, 2X/DAY 0 1000 MG BID
125798331 12579833 3 C TRIATEC /00885601/ RAMIPRIL 1 Oral 5 MG, 2X/DAY 0 5 MG BID
125798331 12579833 4 C ADALAT NIFEDIPINE 1 Oral 30 MG, 1X/DAY 0 30 MG QD
125798331 12579833 5 C SINTROM ACENOCOUMAROL 1 Oral 4 MG, 1X/DAY 0 4 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125798331 12579833 1 Type V hyperlipidaemia
125798331 12579833 2 Diabetes mellitus
125798331 12579833 3 Hypertension
125798331 12579833 4 Hypertension
125798331 12579833 5 Aortic valve replacement

Outcome of event

Event ID CASEID OUTC COD
125798331 12579833 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125798331 12579833 Abasia
125798331 12579833 Pain

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
125798331 12579833 1 201208 201210 0
125798331 12579833 2 201102 0
125798331 12579833 3 201011 0
125798331 12579833 4 201011 0
125798331 12579833 5 201011 0