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
123711222 12371122 2 F 20160905 20160516 20160919 EXP PL-AUROBINDO-AUR-APL-2016-05905 AUROBINDO 0.00 Y 0.00000 20160919 OT PL PL

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
123711222 12371122 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 5 MG, DAILY Y U 78021 5 MG
123711222 12371122 2 I Simvastatin 20mg SIMVASTATIN 1 Unknown 20 MG, DAILY Y U 0 20 MG
123711222 12371122 3 C PERINDOPRIL PERINDOPRIL 1 Unknown 10 MG, UNK Y U 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123711222 12371122 1 Product used for unknown indication
123711222 12371122 2 Type V hyperlipidaemia
123711222 12371122 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123711222 12371122 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123711222 12371122 Asthenia
123711222 12371122 Confusional state
123711222 12371122 Depression
123711222 12371122 Dizziness
123711222 12371122 Drug interaction
123711222 12371122 Fatigue
123711222 12371122 Hypokinesia
123711222 12371122 Muscular weakness
123711222 12371122 Myalgia

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

no results found

Therapies reported

no results found