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
887415112 8874151 12 F 2007 20160708 20121023 20160713 EXP BR-ROCHE-700688 ROCHE 43.82 YR F Y 60.00000 KG 20160713 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
887415112 8874151 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) Y 103705 SOLUTION FOR INFUSION
887415112 8874151 2 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) Y 103705 SOLUTION FOR INFUSION
887415112 8874151 3 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) Y 103705 SOLUTION FOR INFUSION
887415112 8874151 4 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) MOST RECENT INFUSION ON 29/APR/2016 Y 103705 SOLUTION FOR INFUSION
887415112 8874151 5 SS RIVOTRIL CLONAZEPAM 1 Unknown U 17533 2 MG
887415112 8874151 6 SS PHENERGAN PROMETHAZINE HYDROCHLORIDE 1 Unknown U 0
887415112 8874151 7 SS PROPANOLOL PROPRANOLOL HYDROCHLORIDE 1 Unknown U 0 40 MG TABLET QD
887415112 8874151 8 C SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATE 1 0
887415112 8874151 9 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Unknown 0 40 MG TABLET QD
887415112 8874151 10 C CORTISONE CORTISONEHYDROCORTISONE 1 Unknown 0 5 MG
887415112 8874151 11 C SERTRALINE SERTRALINE HYDROCHLORIDE 1 Unknown 0 5 MG
887415112 8874151 12 C ESCITALOPRAM ESCITALOPRAM OXALATE 1 Unknown 0 10 MG
887415112 8874151 13 C BRINZOLAMID 2 0
887415112 8874151 14 C METICORTEN PREDNISONE 1 Unknown 0 5 MG TABLET BID
887415112 8874151 15 C METICORTEN PREDNISONE 1 Unknown 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
887415112 8874151 1 Rheumatoid arthritis
887415112 8874151 5 Insomnia
887415112 8874151 6 Premedication
887415112 8874151 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
887415112 8874151 HO
887415112 8874151 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
887415112 8874151 Arrhythmia
887415112 8874151 Arthralgia
887415112 8874151 Arthrodesis
887415112 8874151 Blood pressure decreased
887415112 8874151 Candida infection
887415112 8874151 Chest pain
887415112 8874151 Dengue fever
887415112 8874151 Depression
887415112 8874151 Fatigue
887415112 8874151 Haematoma
887415112 8874151 Hyperhidrosis
887415112 8874151 Hypersensitivity
887415112 8874151 Ill-defined disorder
887415112 8874151 Laryngeal disorder
887415112 8874151 Local swelling
887415112 8874151 Medication error
887415112 8874151 Musculoskeletal stiffness
887415112 8874151 Nodule
887415112 8874151 Oral herpes
887415112 8874151 Pain
887415112 8874151 Pain in extremity
887415112 8874151 Peripheral swelling
887415112 8874151 Rhinitis
887415112 8874151 Sinusitis
887415112 8874151 Somnolence
887415112 8874151 Tachycardia
887415112 8874151 Visual impairment
887415112 8874151 Weight increased

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
887415112 8874151 3 20120401 20120430 0