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
5577633 6463711 F 5577633-2 20060501 20071220 20071231 EXP PHBS2007JP18404 NOVARTIS PHARMACEUTICALS CORP. 54 YR F Y 46 KG 20071229 OT 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
5577633 1009349341 PS VOLTAREN 1 RECTAL 25 MG/DAY 019201
5577633 1009349342 SS DICLOFENAC SODIUM 1 ORAL 75 MG/DAY
5577633 1009349343 C RANITAC 2 ORAL 225 MG/DAY
5577633 1009349344 C DOMPERIDONE 2 ORAL 30 MG/DAY
5577633 1009349345 C MINOMYCIN 2 ORAL 50 MG/DAY
5577633 1009349346 C KETOTIFEN FUMARATE 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
5577633 1009349341 PYREXIA
5577633 1009349342 HEADACHE
5577633 1009349343 ABDOMINAL PAIN UPPER
5577633 1009349344 NAUSEA

Outcome of event

Event ID OUTC COD
5577633 DS
5577633 OT

Reactions reported

Event ID PT
5577633 ALANINE AMINOTRANSFERASE INCREASED
5577633 ASPARTATE AMINOTRANSFERASE INCREASED
5577633 BLOOD BILIRUBIN INCREASED
5577633 C-REACTIVE PROTEIN INCREASED
5577633 CONJUNCTIVITIS
5577633 CORNEAL DISORDER
5577633 EYE PAIN
5577633 GAMMA-GLUTAMYLTRANSFERASE INCREASED
5577633 LACRIMATION DECREASED
5577633 LIVER DISORDER
5577633 OCULAR HYPERAEMIA
5577633 STEVENS-JOHNSON SYNDROME
5577633 VISION BLURRED

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
5577633 1009349341 20060514 20060515 2880 MIN
5577633 1009349342 20060512 20060512 1440 MIN
5577633 1009349343 20060512 20060512 1440 MIN
5577633 1009349344 20060512 20060512 1440 MIN
5577633 1009349345 20060511 20060511 1440 MIN
5577633 1009349346 20060511 20060511 1440 MIN