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
6545512 6949515 F 6545512-X 20100118 20100121 EXP GB-WYE-H08646309 WYETH PHARMACEUTICALS INC. 9 YR M Y 20100121 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
6545512 1012977314 I RAPAMUNE 1 21110
6545512 1012977315 I PREDNISOLONE 1
6545512 1012977316 PS LAMIVUDINE 2 ORAL
6545512 1012977317 SS ZIDOVUDINE 1 ORAL
6545512 1012977318 SS SUSTIVA 1 ORAL
6545512 1012977319 SS COTRIM 1 NOT PROVIDED
6545512 1012977320 SS DIDANOSINE 1 NOT PROVIDED
6545512 1012977321 SS ABACAVIR SULFATE AND LAMIVUDINE 1
6545512 1012977322 SS NELFINAVIR MESYLATE 1 NOT PROVIDED
6545512 1012977323 I MYCOPHENOLATE MOFETIL 1
6545512 1012977324 SS ABACAVIR 1 NOT PROVIDED

Indications of drugs used

Event ID DRUG SEQ INDI PT
6545512 1012977314 PROPHYLAXIS AGAINST TRANSPLANT REJECTION
6545512 1012977315 PROPHYLAXIS AGAINST TRANSPLANT REJECTION
6545512 1012977316 ANTIRETROVIRAL THERAPY
6545512 1012977317 ANTIRETROVIRAL THERAPY
6545512 1012977318 ANTIRETROVIRAL THERAPY
6545512 1012977323 PROPHYLAXIS AGAINST TRANSPLANT REJECTION

Outcome of event

Event ID OUTC COD
6545512 HO

Reactions reported

Event ID PT
6545512 CHOLESTASIS
6545512 DISEASE RECURRENCE
6545512 DRUG INEFFECTIVE
6545512 DRUG INTERACTION
6545512 HIV INFECTION
6545512 HYPERLIPIDAEMIA
6545512 HYPERTENSION
6545512 MYOPATHY
6545512 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
6545512 1012977316 20070330 20070701
6545512 1012977317 20070330 20070701
6545512 1012977318 20070302 20070701