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
127361962 12736196 2 F 20160905 20160913 20160917 EXP DE-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-123491 RANBAXY 0.00 M Y 103.00000 KG 20160917 CN ES DE

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
127361962 12736196 1 SS PRAVASTATIN. PRAVASTATIN 1 Oral 1 DF, DAILY Y U 0 1 DF
127361962 12736196 2 PS SIMVASTATIN. SIMVASTATIN 1 Oral UNK Y U 76285
127361962 12736196 3 SS Atorvastatin ATORVASTATIN 1 Oral 1 DF, QD Y U 0 1 DF
127361962 12736196 4 SS FENOFIBRATE. FENOFIBRATE 1 Oral 1 DF, QD U U 0 1 DF
127361962 12736196 5 C OMEGA-3 ACIDS OMEGA-3 FATTY ACIDS 1 Unknown 1000 MG, TID U U 0 1000 MG Q8H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127361962 12736196 1 Hypercholesterolaemia
127361962 12736196 2 Hypercholesterolaemia
127361962 12736196 3 Hypercholesterolaemia
127361962 12736196 4 Hypercholesterolaemia
127361962 12736196 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127361962 12736196 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127361962 12736196 Arthralgia
127361962 12736196 Gout
127361962 12736196 Petechiae
127361962 12736196 Skin exfoliation
127361962 12736196 Tendon injury

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
127361962 12736196 1 20160223 20160406 0
127361962 12736196 3 20160218 20160223 0
127361962 12736196 4 20160614 20160810 0