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
6534446 6949515 F 6534446-2 20100104 20100112 EXP GB-WYE-H08646309 WYETH PHARMACEUTICALS INC. 9 YR M Y 20100112 OT UNITED KINGDOM

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
6534446 1012930893 I RAPAMUNE 1 21110
6534446 1012930894 I PREDNISOLONE 1
6534446 1012930895 PS LAMIVUDINE 2 NOT PROVIDED
6534446 1012930896 SS ZIDOVUDINE 1
6534446 1012930897 SS SUSTIVA 1 NOT PROVIDED
6534446 1012930898 SS COTRIM 1
6534446 1012930899 SS DIDANOSINE 1
6534446 1012930900 SS ABACAVIR SULFATE AND LAMIVUDINE 1
6534446 1012930901 SS NELFINAVIR MESYLATE 1
6534446 1012930902 I MYCOPHENOLATE MOFETIL 1
6534446 1012930903 SS ABACAVIR 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6534446 1012930893 PROPHYLAXIS AGAINST TRANSPLANT REJECTION
6534446 1012930894 PROPHYLAXIS AGAINST TRANSPLANT REJECTION
6534446 1012930895 ANTIRETROVIRAL THERAPY
6534446 1012930896 ANTIRETROVIRAL THERAPY
6534446 1012930897 ANTIRETROVIRAL THERAPY
6534446 1012930902 PROPHYLAXIS AGAINST TRANSPLANT REJECTION

Outcome of event

Event ID OUTC COD
6534446 HO

Reactions reported

Event ID PT
6534446 CHOLESTASIS
6534446 DISEASE RECURRENCE
6534446 DRUG INEFFECTIVE
6534446 DRUG INTERACTION
6534446 HIV INFECTION
6534446 HYPERLIPIDAEMIA
6534446 HYPERTENSION
6534446 MYOPATHY
6534446 RENAL IMPAIRMENT

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
6534446 1012930895 20070330 20070701
6534446 1012930897 20070302 20070701