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
6733698 7394373 I 6733698-3 20100512 20100520 EXP OM-BAYER-201025135GPV BAYER HEALTHCARE LLC 38 YR M Y 20100520 OT OMAN

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
6733698 1013720713 PS ASPIRIN 1 UNKNOWN 021317
6733698 1013720714 SS CLOPIDOGREL 1 UNKNOWN
6733698 1013720715 SS CLOPIDOGREL 1 UNKNOWN
6733698 1013720716 C ATENOLOL 1 UNKNOWN
6733698 1013720717 C SIMVASTATIN 1 UNKNOWN
6733698 1013720718 C TIROFIBAN 2 UNKNOWN
6733698 1013720719 C TIROFIBAN 2 UNKNOWN
6733698 1013720720 C UNFRACTIONED HEPARIN 2 UNKNOWN
6733698 1013720721 C UNFRACTIONED HEPARIN 2 UNKNOWN
6733698 1013720722 C UNFRACTIONED HEPARIN 2 UNKNOWN
6733698 1013720723 C ENOXAPARIN SODIUM 1 UNKNOWN
6733698 1013720724 C RETEPLASE 2 INTRAVENOUS BOLUS 10 UNITS OF RETEPLASE

Indications of drugs used

Event ID DRUG SEQ INDI PT
6733698 1013720713 MYOCARDIAL INFARCTION
6733698 1013720714 MYOCARDIAL INFARCTION
6733698 1013720716 MYOCARDIAL INFARCTION
6733698 1013720717 MYOCARDIAL INFARCTION
6733698 1013720718 ANTICOAGULANT THERAPY
6733698 1013720720 ANTICOAGULANT THERAPY
6733698 1013720723 ANTICOAGULANT THERAPY
6733698 1013720724 THROMBOLYSIS

Outcome of event

Event ID OUTC COD
6733698 HO
6733698 OT

Reactions reported

Event ID PT
6733698 CEREBRAL HAEMATOMA
6733698 CORONARY ARTERY OCCLUSION
6733698 PULMONARY EMBOLISM

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6733698 1013720719 24 HR
6733698 1013720722 24 HR