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
127204261 12720426 1 I 20160825 20160907 20160907 EXP IT-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-123164 RANBAXY 0.00 F Y 79.00000 KG 20160907 OT 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
127204261 12720426 1 SS PRAVASTATIN. PRAVASTATIN 1 Unknown Y U 0
127204261 12720426 2 PS SIMVASTATIN. SIMVASTATIN 1 Unknown Y U 76285
127204261 12720426 3 SS Atorvastatin ATORVASTATIN 1 Oral Y U 0
127204261 12720426 4 SS ROSUVASTATIN. ROSUVASTATIN 1 Unknown Y U 0
127204261 12720426 5 C EUTIROX LEVOTHYROXINE SODIUM 1 Unknown U U 0
127204261 12720426 6 C LOBIVON 5 MG 2 Unknown U U 0
127204261 12720426 7 C EZETROL 10 MG 2 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127204261 12720426 1 Type IIa hyperlipidaemia
127204261 12720426 2 Type IIa hyperlipidaemia
127204261 12720426 3 Type IIa hyperlipidaemia
127204261 12720426 4 Type IIa hyperlipidaemia
127204261 12720426 5 Autoimmune thyroiditis
127204261 12720426 6 Hypertension
127204261 12720426 7 Type IIa hyperlipidaemia

Outcome of event

Event ID CASEID OUTC COD
127204261 12720426 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127204261 12720426 Myopathy
127204261 12720426 Pain

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

no results found

Therapies reported

no results found