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
127110902 12711090 2 F 20160501 20160829 20160902 20160907 EXP FR-PFIZER INC-2016405968 PFIZER 65.00 YR M Y 0.00000 20160907 OT FR FR

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
127110902 12711090 1 PS TAHOR ATORVASTATIN CALCIUM 1 Oral 40 MG, 1X/DAY (IN THE EVENING) 20702 40 MG QD
127110902 12711090 2 SS Triatec RAMIPRIL 1 Oral 2.5 MG, 2X/DAY (IN THE MORNING AND IN THE EVENING) 19901 2.5 MG BID
127110902 12711090 3 SS ATENOLOL. ATENOLOL 1 Oral 25 MG, 1X/DAY 0 25 MG QD
127110902 12711090 4 SS ATARAX HYDROXYZINEHYDROXYZINE HYDROCHLORIDE 1 Oral 25 MG, 1X/DAY 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127110902 12711090 1 Hypercholesterolaemia
127110902 12711090 2 Cardiac failure
127110902 12711090 3 Cardiac failure

Outcome of event

Event ID CASEID OUTC COD
127110902 12711090 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127110902 12711090 Interstitial lung disease

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
127110902 12711090 1 20020701 0
127110902 12711090 2 20020701 0
127110902 12711090 3 20020701 0
127110902 12711090 4 20040521 0