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
6523392 7178898 F 6523392-6 20091102 20091217 20091231 EXP ZM-BRISTOL-MYERS SQUIBB COMPANY-14857783 BRISTOL-MYERS SQUIBB COMPANY 32 YR M Y 20091231 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
6523392 1012885614 PS EFAVIRENZ 1 ORAL INTERRUPTED ON 02NOV2009; 132 DAYS 20972
6523392 1012885615 SS TENOFOVIR DISOPROXIL FUMARATE 1 ORAL INTERRUPTED ON 02NOV2009; 132 DAYS
6523392 1012885616 SS EMTRICITABINE 2 ORAL INTERRUPTED ON 02NOV2009; 132 DAYS
6523392 1012885617 SS ETHAMBUTOL HYDROCHLORIDE 1 ORAL CONTINUATION PHASE FROM 07-SEP-2009
6523392 1012885618 SS ISONIAZID 1 ORAL
6523392 1012885619 SS PYRAZINAMIDE 1 ORAL CONTINUATION PHASE FROM 07-SEP-2009
6523392 1012885620 SS RIFAMPIN 1 ORAL
6523392 1012885621 C SULFAMETHOXAZOLE AND TRIMETHOPRIM 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6523392 1012885614 HIV INFECTION
6523392 1012885615 HIV INFECTION
6523392 1012885616 HIV INFECTION
6523392 1012885617 TUBERCULOSIS
6523392 1012885618 TUBERCULOSIS
6523392 1012885619 TUBERCULOSIS
6523392 1012885620 TUBERCULOSIS

Outcome of event

Event ID OUTC COD
6523392 LT

Reactions reported

Event ID PT
6523392 HEPATITIS
6523392 NEUTROPENIA

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
6523392 1012885614 20090624
6523392 1012885615 20090624
6523392 1012885616 20090624
6523392 1012885617 20090618 20090906
6523392 1012885618 20090618
6523392 1012885619 20090618 20090906
6523392 1012885620 20090618