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
126740291 12674029 1 I 20160526 20160812 20160822 20160822 EXP IT-MINISAL02-371152 IT-MYLANLABS-2016M1034486 MYLAN 0.00 Y 0.00000 20160822 PH 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
126740291 12674029 1 PS ATENOLOL. ATENOLOL 1 Oral 50 MG, QD 1300 MG Y U 73457 50 MG QD
126740291 12674029 2 C CARDIRENE ASPIRIN DL-LYSINE 1 Oral 1 DF 0 1 DF POWDER FOR SOLUTION FOR INFUSION
126740291 12674029 3 C PLAVIX CLOPIDOGREL BISULFATE 1 Oral 1 DF 0 1 DF
126740291 12674029 4 C TOTALIP ATORVASTATIN 1 Oral 1 DF 0 1 DF
126740291 12674029 5 C BIFRIL COMP 2 1 DF 0 1 DF FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126740291 12674029 1 Hypertension
126740291 12674029 2 Product used for unknown indication
126740291 12674029 3 Product used for unknown indication
126740291 12674029 4 Product used for unknown indication
126740291 12674029 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126740291 12674029 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126740291 12674029 Bradycardia
126740291 12674029 Electrocardiogram abnormal
126740291 12674029 Syncope

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126740291 12674029 1 20160501 20160526 0