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
6138274 6956713 I 6138274-1 20080115 20090327 20090331 EXP B0567246A GLAXOSMITHKLINE 72 M Y 20090331 CN FRANCE

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
6138274 1011356967 PS AUGMENTIN '125' 1 ORAL 3G PER DAY UNKNOWN 50564
6138274 1011356968 SS MINOCIN 1 ORAL 1CAP PER DAY UNKNOWN
6138274 1011356969 SS DOLIPRANE 2 ORAL 3G PER DAY UNKNOWN
6138274 1011356970 SS DIMETANE 1 ORAL UNKNOWN
6138274 1011356971 C CARDENSIEL 2 ORAL UNKNOWN
6138274 1011356972 C ULTRALEVURE 2 UNKNOWN 200MG PER DAY UNKNOWN
6138274 1011356973 C BRONCHOKOD 2 UNKNOWN UNKNOWN
6138274 1011356974 C CORTANCYL 2 UNKNOWN 60MG PER DAY UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
6138274 1011356967 BRONCHITIS
6138274 1011356968 BRONCHITIS
6138274 1011356969 BRONCHITIS
6138274 1011356970 BRONCHITIS

Outcome of event

Event ID OUTC COD
6138274 OT

Reactions reported

Event ID PT
6138274 CELL DEATH
6138274 CHROMATURIA
6138274 HEPATITIS CHOLESTATIC
6138274 JAUNDICE
6138274 MIXED LIVER INJURY
6138274 RED BLOOD CELL SEDIMENTATION RATE INCREASED
6138274 TRANSAMINASES INCREASED

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
6138274 1011356967 20081206 20081223 18 DAY
6138274 1011356968 20090102 20090105 4 DAY
6138274 1011356969 20081206 20090103 29 DAY
6138274 1011356970 20081220 20090108 20 DAY
6138274 1011356972 20081206 20081223 18 DAY
6138274 1011356973 20081206 20081216 11 DAY
6138274 1011356974 20081220 20081227 8 DAY