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
4869989 5953740 F 4869989-0 20031218 20040528 20051231 EXP FR-BOEHRINGER INGELHEIM PHARMACEUTICALS, INC.-2004-FF-00342FF BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. M Y 78 KG 20051231 FRANCE

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
4869989 1006778357 PS TIPRANAVIR + RITONAVIR CO-ADMIN 2 ORAL TPV/RTV 500/200 MG B.I.D.
4869989 1006778358 C TENOFOVIR 2 ORAL
4869989 1006778359 C DIDANOSINE 1 ORAL
4869989 1006778360 C LAMIVUDINE 1 ORAL
4869989 1006778361 C EFAVIRENZ 1 ORAL
4869989 1006778362 C BEDELIX 2 UNKNOWN
4869989 1006778363 C CEPHYL 2 UNKNOWN
4869989 1006778364 C CARBOLEVURE 2 UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
4869989 1006778357 HIV INFECTION
4869989 1006778358 HIV INFECTION
4869989 1006778359 HIV INFECTION
4869989 1006778360 HIV INFECTION
4869989 1006778361 HIV INFECTION
4869989 1006778362 FLATULENCE
4869989 1006778363 HEADACHE
4869989 1006778364 FLATULENCE

Outcome of event

Event ID OUTC COD
4869989 HO

Reactions reported

Event ID PT
4869989 CHOLANGITIS CHRONIC
4869989 DIARRHOEA
4869989 FLATULENCE
4869989 GINGIVITIS
4869989 HEPATIC STEATOSIS

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
4869989 1006778357 20030904
4869989 1006778358 20011206
4869989 1006778359 20000901
4869989 1006778360 20011001
4869989 1006778361 20030918
4869989 1006778362 20031218
4869989 1006778363 20031218
4869989 1006778364 20040219