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
126439921 12643992 1 I 20160407 20160802 20160811 20160811 EXP FR-PFIZER INC-2016371560 PFIZER 83.00 YR M Y 0.00000 20160811 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
126439921 12643992 1 PS Fragmine DALTEPARIN SODIUM 1 Subcutaneous 0.2 ML, 1X/DAY 2 ML Y 20287 .2 ML SOLUTION FOR INJECTION QD
126439921 12643992 2 C COOLMETEC HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 0
126439921 12643992 3 C LERCAN LERCANIDIPINE 1 0
126439921 12643992 4 C UROREC SILODOSIN 1 0
126439921 12643992 5 C PARIET RABEPRAZOLE SODIUM 1 0
126439921 12643992 6 C URISPAS FLAVOXATE HYDROCHLORIDE 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126439921 12643992 HO
126439921 12643992 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126439921 12643992 Anaemia
126439921 12643992 Gastrointestinal haemorrhage
126439921 12643992 Shock haemorrhagic

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
126439921 12643992 1 20160331 20160408 0