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
6387730 7151026 I 6387730-X 20090717 20090915 20090930 EXP GXBR2009US01874 SANDOZ, INC. 86 YR M N 20090929 MD UNITED STATES

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
6387730 1012374773 PS RIFAMPIN 1 ORAL , ORAL 64150
6387730 1012432449 SS ISONIAZID 1 ORAL ,ORAL
6387730 1012432450 SS PYRAZINAMIDE 1 ORAL , ORAL U U
6387730 1012432451 SS ETHAMBUTOL (ETHAMBUTOL) 2 ORAL , ORAL U U

Indications of drugs used

Event ID DRUG SEQ INDI PT
6387730 1012374773 TUBERCULOSIS
6387730 1012432449 TUBERCULOSIS
6387730 1012432450 TUBERCULOSIS
6387730 1012432451 TUBERCULOSIS

Outcome of event

Event ID OUTC COD
6387730 HO

Reactions reported

Event ID PT
6387730 ACUTE MYOCARDIAL INFARCTION
6387730 DYSPNOEA
6387730 HYPOTENSION
6387730 MYOCARDIAL INFARCTION
6387730 PNEUMONITIS
6387730 PULMONARY FIBROSIS
6387730 SEPSIS
6387730 STAPHYLOCOCCAL INFECTION
6387730 SYSTEMIC INFLAMMATORY RESPONSE SYNDROME

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

Event ID RPSR COD
6387730 HP
6387730 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6387730 1012374773 20090716
6387730 1012432449 20090716
6387730 1012432450 20090716
6387730 1012432451 20090716