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
127046421 12704642 1 I 20091123 20160825 20160831 20160831 EXP PHHY2016IT117870 SANDOZ 48.89 YR F Y 0.00000 20160831 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
127046421 12704642 1 PS SIMVASTATIN. SIMVASTATIN 1 Unknown U 77766
127046421 12704642 2 SS ATORVASTATIN ATORVASTATIN 1 Unknown U 0
127046421 12704642 3 SS PRAVASTATIN. PRAVASTATIN 1 Unknown U 0
127046421 12704642 4 SS ROSUVASTATIN. ROSUVASTATIN 1 Unknown U 0
127046421 12704642 5 C LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown U 0
127046421 12704642 6 C OLMESARTAN OLMESARTAN 1 Unknown U 0
127046421 12704642 7 C MONACOLIN K//LOVASTATIN 2 3 MG, UNK 0 3 MG
127046421 12704642 8 C MONACOLIN K//LOVASTATIN 2 0
127046421 12704642 9 C MONACOLIN K//LOVASTATIN 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127046421 12704642 1 Type IIa hyperlipidaemia
127046421 12704642 2 Type IIa hyperlipidaemia
127046421 12704642 3 Type IIa hyperlipidaemia
127046421 12704642 4 Type IIa hyperlipidaemia
127046421 12704642 5 Product used for unknown indication
127046421 12704642 6 Product used for unknown indication
127046421 12704642 7 Type IIa hyperlipidaemia
127046421 12704642 8 Hypertension
127046421 12704642 9 Obesity

Outcome of event

Event ID CASEID OUTC COD
127046421 12704642 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127046421 12704642 Myopathy
127046421 12704642 Pain in extremity

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

no results found

Therapies reported

no results found