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
4358398 5722837 I 4358398-9 20031216 20040430 20040511 EXP K200400656 KING PHARMACEUTICALS, INC. 75 YR F N 87 KG 20040510 OT

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
4358398 1004862372 PS ALTACE 1 ORAL ORAL Y D 19901
4358398 1004875742 SS LEVOFLOXACIN 1 ORAL SEE IMAGE, ORAL Y D
4358398 1004875746 SS OFLOXACIN 1 INTRAVENOUS INTRAVENOUS Y D
4358398 1004875749 C AUGMENTIN 1
4358398 1004875753 C ROCEPHIN 1
4358398 1004875754 C OMEPRAZOLE 1
4358398 1004875755 C DIGOXIN 1
4358398 1004875756 C CORDARONE 1
4358398 1004875758 C PREVISCAN (FLUINDIONE) 2
4358398 1004875763 C FRAXIPARINE (HEPARIN-FRACTION, CALCIUM SALT) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
4358398 1004875742 PNEUMONIA
4358398 1004875746 PNEUMONIA

Outcome of event

Event ID OUTC COD
4358398 HO

Reactions reported

Event ID PT
4358398 DIARRHOEA
4358398 DRUG TOXICITY
4358398 ENTEROBACTER INFECTION
4358398 GASTROENTERITIS STAPHYLOCOCCAL
4358398 PYELONEPHRITIS
4358398 RENAL FAILURE ACUTE

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

Event ID RPSR COD
4358398 FGN
4358398 HP
4358398 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4358398 1004862372 20031218 20031229
4358398 1004875742 20031219 20031220
4358398 1004875742 20031221 20031226
4358398 1004875746 20031215 20031219