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
127205311 12720531 1 I 20091123 20160826 20160907 20160907 EXP IT-APOTEX-2016AP011028 APOTEX 48.89 YR F Y 0.00000 20160907 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
127205311 12720531 1 SS PRAVASTATINA DOC GENERICI PRAVASTATIN SODIUM 1 Unknown UNK Y 0 TABLET
127205311 12720531 2 SS SIMVASTATINA DOC GENERICI SIMVASTATIN 1 Unknown UNK Y 0 TABLET
127205311 12720531 3 PS ATORVASTATINA DOC GENERICI COMPRESSE RIVESTITE CON FILM ATORVASTATIN 1 Unknown UNK Y 90548 TABLET
127205311 12720531 4 SS ROSUVASTATIN CALCIUM. ROSUVASTATIN CALCIUM 1 Unknown UNK Y U 0
127205311 12720531 5 C LEVOTHYROXINE SODIUM. LEVOTHYROXINE SODIUM 1 Unknown UNK U U 0
127205311 12720531 6 C OLMESARTAN MEDOXOMIL. OLMESARTAN MEDOXOMIL 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127205311 12720531 1 Type IIa hyperlipidaemia
127205311 12720531 2 Type IIa hyperlipidaemia
127205311 12720531 3 Type IIa hyperlipidaemia
127205311 12720531 4 Type IIa hyperlipidaemia
127205311 12720531 5 Product used for unknown indication
127205311 12720531 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127205311 12720531 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127205311 12720531 Asthenia
127205311 12720531 Myopathy
127205311 12720531 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