The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
86187413 8618741 3 F 2010 20160906 20120618 20160912 EXP BR-JNJFOC-20120605023 JANSSEN 0.00 E F Y 70.00000 KG 20160912 CN BR BR

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
86187413 8618741 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) Y U NOT REQUIRED 0 LYOPHILIZED POWDER
86187413 8618741 2 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) Y U NOT REQUIRED 103772 LYOPHILIZED POWDER
86187413 8618741 3 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Unknown 0 UNSPECIFIED
86187413 8618741 4 C SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown 0 UNSPECIFIED
86187413 8618741 5 C IMURAN AZATHIOPRINE 1 Unknown 0 50 MG UNSPECIFIED
86187413 8618741 6 C RIVOTRIL CLONAZEPAM 1 Unknown 0 UNSPECIFIED
86187413 8618741 7 C EXELON RIVASTIGMINE TARTRATE 1 Unknown 0 UNSPECIFIED
86187413 8618741 8 C ZIDER MEMANTINE HYDROCHLORIDE 1 Unknown 0 10 MG UNSPECIFIED
86187413 8618741 9 C ANCORON AMIODARONE HYDROCHLORIDE 1 Unknown 0 100 MG UNSPECIFIED
86187413 8618741 10 C QUEROPAX QUETIAPINE FUMARATE 1 Unknown 0 UNSPECIFIED
86187413 8618741 11 C PROPANOLOL PROPRANOLOL HYDROCHLORIDE 1 Unknown 0 40 MG UNSPECIFIED
86187413 8618741 12 C LEVOID LEVOTHYROXINE 1 Unknown 0 100 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
86187413 8618741 1 Crohn's disease
86187413 8618741 2 Rheumatoid arthritis
86187413 8618741 3 Gastrointestinal disorder therapy
86187413 8618741 4 Thyroid disorder
86187413 8618741 5 Rheumatoid arthritis
86187413 8618741 6 Sleep disorder therapy

Outcome of event

Event ID CASEID OUTC COD
86187413 8618741 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
86187413 8618741 Arrhythmia
86187413 8618741 Dementia Alzheimer's type
86187413 8618741 Drug effect decreased
86187413 8618741 Eye operation
86187413 8618741 Feeding disorder
86187413 8618741 Food poisoning
86187413 8618741 Gait disturbance
86187413 8618741 Hernia
86187413 8618741 Hypertension
86187413 8618741 Inadequate lubrication
86187413 8618741 Ocular hyperaemia

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
86187413 8618741 1 2007 0
86187413 8618741 2 2007 0
86187413 8618741 5 2007 0