The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6202952 7008098 I 6202952-6 20090106 20090507 20090519 EXP 2009AP001868 APOTEX INC. 79 YR F N 20090518 UNITED KINGDOM

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6202952 1011628955 PS CLARITHROMYCIN 1 ORAL 500 MG;BID; PO D D 65384
6202952 1011658442 SS SIMVASTATIN 1 ORAL 80 MG; PO D D
6202952 1011658443 C BISOPROLOL FUMARATE 1
6202952 1011658444 C FERROUS SULPHATE (FERROUS SULFATE) 2
6202952 1011658445 C FUROSEMIDE 1
6202952 1011658487 C GLYCERYL TRINITRATE (GLYCERYL TRINITRATE) 2
6202952 1011658503 C ISOSORBIDE MONONITRATE 1
6202952 1011658505 C NICORANDIL (NICORANDIL) 2
6202952 1011658506 C OMEPRAZOLE 1
6202952 1011658507 C RAMIPRIL 1
6202952 1011658508 C WARFARIN SODIUM 1
6202952 1011658509 C ZOPICLONE (ZOPICLONE) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6202952 1011628955 BRONCHITIS
6202952 1011658442 MYOCARDIAL ISCHAEMIA

Outcome of event

Event ID OUTC COD
6202952 DE

Reactions reported

Event ID PT
6202952 BLOOD CREATINE PHOSPHOKINASE INCREASED
6202952 CEREBROVASCULAR ACCIDENT
6202952 DRUG INTERACTION
6202952 MYOSITIS
6202952 SYNCOPE

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

Event ID RPSR COD
6202952 HP
6202952 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6202952 1011628955 20081224 20081231 8 DAY
6202952 1011658442 20050513 20090113