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
4338803 5717653 I 4338803-4 20040207 20040330 20040409 EXP JP-JNJFOC-20040306396 JOHNSON + JOHNSON PHARMACEUTICAL 44 YR M N 20040408 MD

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
4338803 1004786467 PS OFLOXACIN 1 INTRAVENOUS 400 MG, INTRAVENOUS U U 20087
4338803 1004798600 SS GANCICLOVIR SODIUM 1 INTRAVENOUS 900 MG, INTRAVENOUS D D
4338803 1004798601 SS CLAVENTIN (CLAVENTIN) 2 INTRAVENOUS 15 G, INTRAVENOUS U U
4338803 1004798602 SS NEORAL 1 ORAL 100 MG, ORAL U U
4338803 1004798607 SS CANCIDAS 1 INTRAVENOUS 50 MG, INTRAVENOUS U U
4338803 1004798610 SS VORICONAZOLE (VORICONAZOLE) 2 INTRAVENOUS 400 MG, INTRAVENOUS U U
4338803 1004798612 SS OFLOXACIN 1 D D
4338803 1004798613 C VANCOMYCIN 1
4338803 1004798614 C AMBISOME 1

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
4338803 DE
4338803 HO

Reactions reported

Event ID PT
4338803 ACIDOSIS
4338803 ASPERGILLOSIS
4338803 ENCEPHALOPATHY
4338803 MULTI-ORGAN FAILURE
4338803 MUSCLE RIGIDITY
4338803 MYOCLONUS
4338803 RENAL FAILURE
4338803 TREMOR

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

Event ID RPSR COD
4338803 FGN
4338803 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4338803 1004786467 20040129 20040207
4338803 1004798600 20040121 20040207
4338803 1004798601 20040121 20040207
4338803 1004798602 20031219 20040222
4338803 1004798607 20040121 20040207
4338803 1004798610 20040105 20040210
4338803 1004798612 20031219 20031226