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
4542780 3571955 F 4542780-0 20000914 20001110 20041231 EXP 200022074US AVENTIS PHARMACEUTICALS, INC. F Y 65.5 KG 20041231 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
4542780 1005546978 PS ARAVA 1 ORAL UNK
4542780 1005546979 C METHOTREXATE 1 DOSE: 2.5 TABS: SIX TABS UNK
4542780 1005546980 C LEUCOVORIN 2 UNK
4542780 1005546981 C FELDENE 1 UNK
4542780 1005546982 C CALCIUM CARBONATE 2 UNK
4542780 1005546983 C TYLENOL W/ CODEINE NO. 3 1 DOSE: ONE TO TWO Q6H UNK
4542780 1005546984 C FLOVENT 1 DOSE: 2 PUFFS UNK
4542780 1005546985 C IRON SULFATETHIAMIN COMPOUND TAB 1 UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
4542780 1005546978 RHEUMATOID ARTHRITIS
4542780 1005546981 RASH
4542780 1005546983 ARTHRALGIA
4542780 1005546984 BRONCHOSPASM

Outcome of event

Event ID OUTC COD
4542780 HO
4542780 OT

Reactions reported

Event ID PT
4542780 ABDOMINAL PAIN
4542780 ATRIAL FLUTTER
4542780 BLOOD ALKALINE PHOSPHATASE INCREASED
4542780 CARDIAC FAILURE CONGESTIVE
4542780 CARDIOMYOPATHY
4542780 DEEP VEIN THROMBOSIS
4542780 EJECTION FRACTION
4542780 HEPATOMEGALY
4542780 HYPERTENSION
4542780 LUNG INFILTRATION
4542780 PLEURAL EFFUSION
4542780 PNEUMONIA
4542780 PULMONARY EMBOLISM
4542780 PYREXIA

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

Event ID RPSR COD
4542780 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4542780 1005546978 19990111 20000926
4542780 1005546979 20001129