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
5195441 6188109 F 5195441-1 20061113 20061206 20061230 EXP JP-ABBOTT-06P-087-0352717-00 ABBOTT M Y 29.6 KG 20061230 MD JAPAN

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
5195441 1007999457 PS KLARICID 2 ORAL UNKNOWN 50662
5195441 1007999458 SS CLARITHROMYCIN 1 ORAL UNKNOWN 050662
5195441 1007999459 C ERYTHROMYCIN 1 UNKNOWN 061621
5195441 1007999460 C MEQUITAZINE 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
5195441 1007999457 DRUG USE FOR UNKNOWN INDICATION
5195441 1007999458 SINUSITIS
5195441 1007999459 DRUG USE FOR UNKNOWN INDICATION
5195441 1007999460 SINUSITIS

Outcome of event

Event ID OUTC COD
5195441 HO

Reactions reported

Event ID PT
5195441 ANAEMIA
5195441 COLITIS ULCERATIVE
5195441 MELAENA

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5195441 1007999458 20050620 20061113
5195441 1007999460 20050620 20061113