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
6818803 7469534 I 6818803-2 20100330 20100617 20100630 EXP IDA-00376 AKRIMAX PHARMACEUTICALS, LLC 86 YR F N 20100625 ITALY

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
6818803 1014042632 PS INDERAL 1 ORAL 30 MG DAILY, ORAL Y D 16418
6818803 1014106870 SS CORDARONE 1 ORAL 200 MG DAILY, ORAL
6818803 1014106970 C PRAVASTATIN SODIUM 1
6818803 1014107033 C ADALAT CC 1
6818803 1014107034 C PRISNA (MESOGLYCAN) 2
6818803 1014107035 C ASPIRIN 1
6818803 1014107036 C CALCIUM CARBONATE 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6818803 1014042632 EXTRASYSTOLES
6818803 1014106870 EXTRASYSTOLES

Outcome of event

Event ID OUTC COD
6818803 HO

Reactions reported

Event ID PT
6818803 BRADYCARDIA
6818803 NODAL RHYTHM
6818803 SUPRAVENTRICULAR EXTRASYSTOLES
6818803 VENTRICULAR EXTRASYSTOLES

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

Event ID RPSR COD
6818803 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6818803 1014042632 20100101 20100330 89 DAY
6818803 1014106870 20100101 20100330 89 YR