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
127231341 12723134 1 I 20160826 20160908 20160908 EXP IT-APOTEX-2016AP011029 APOTEX 0.00 F Y 79.00000 KG 20160908 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
127231341 12723134 1 SS PRAVASTATINA DOC GENERICI PRAVASTATIN SODIUM 1 Unknown UNK Y 0 TABLET
127231341 12723134 2 SS SIMVASTATINA DOC GENERICI SIMVASTATIN 1 Unknown UNK Y 0 TABLET
127231341 12723134 3 PS ATORVASTATINA DOC GENERICI COMPRESSE RIVESTITE CON FILM ATORVASTATIN 1 Oral UNK Y 90548 TABLET
127231341 12723134 4 SS ROSUVASTATIN CALCIUM. ROSUVASTATIN CALCIUM 1 Unknown UNK Y 0
127231341 12723134 5 C EUTIROX LEVOTHYROXINE SODIUM 1 Unknown UNK U U 0
127231341 12723134 6 C LOBIVON NEBIVOLOL HYDROCHLORIDE 1 Unknown UNK U U 0
127231341 12723134 7 C EZETROL EZETIMIBE 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127231341 12723134 1 Type IIa hyperlipidaemia
127231341 12723134 2 Type IIa hyperlipidaemia
127231341 12723134 3 Type IIa hyperlipidaemia
127231341 12723134 4 Type IIa hyperlipidaemia
127231341 12723134 5 Autoimmune thyroiditis
127231341 12723134 6 Hypertension
127231341 12723134 7 Type IIa hyperlipidaemia

Outcome of event

Event ID CASEID OUTC COD
127231341 12723134 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127231341 12723134 Asthenia
127231341 12723134 Myopathy
127231341 12723134 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