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
125563893 12556389 3 F 20160725 20160714 20160729 EXP IT-PFIZER INC-2016337225 PFIZER 72.00 YR M Y 0.00000 20160729 CN IT IT

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
125563893 12556389 1 PS ZOLOFT SERTRALINE HYDROCHLORIDE 1 UNK U 19839
125563893 12556389 2 SS APIDRA INSULIN GLULISINE 1 UNK U 5S372A 0
125563893 12556389 3 SS LANTUS INSULIN GLARGINE 1 6 IU, UNK 0 6 IU
125563893 12556389 4 SS BLOPRESS CANDESARTAN CILEXETIL 1 2X/DAY U 0 BID
125563893 12556389 5 SS MADOPAR BENSERAZIDE HYDROCHLORIDELEVODOPA 1 UNK U 0
125563893 12556389 6 SS AVODART DUTASTERIDE 1 0.5 MG, 1X/DAY (IN THE MORNING) U 0 .5 MG QD
125563893 12556389 7 SS UROREC SILODOSIN 1 0.8 MG, UNK U 0 .8 MG
125563893 12556389 8 SS NEUPRO ROTIGOTINE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125563893 12556389 2 Diabetes mellitus
125563893 12556389 3 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125563893 12556389 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125563893 12556389 Capillary disorder
125563893 12556389 Hypoglycaemia
125563893 12556389 Joint swelling
125563893 12556389 Nausea
125563893 12556389 Paraesthesia
125563893 12556389 Vertigo

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

no results found

Therapies reported

no results found