The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126123542 12612354 2 F 201607 20160808 20160801 20160812 EXP JP-ABBVIE-16P-087-1686036-00 ABBVIE 15.00 YR M Y 0.00000 20160812 PH JP JP

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126123542 12612354 1 PS CLARITHROMYCIN. CLARITHROMYCIN 1 Oral U UNKNOWN 50662 TABLET
126123542 12612354 2 SS LUVOX FLUVOXAMINE MALEATE 1 Oral U UNKNOWN 0 TABLET
126123542 12612354 3 SS PL ACETAMINOPHENCAFFEINEPROMETHAZINESALICYLAMIDE 1 Oral U 0 GRANULES

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126123542 12612354 1 Nasopharyngitis
126123542 12612354 2 Attention deficit/hyperactivity disorder
126123542 12612354 3 Nasopharyngitis

Outcome of event

Event ID CASEID OUTC COD
126123542 12612354 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126123542 12612354 Decreased appetite
126123542 12612354 Electrocardiogram QT prolonged
126123542 12612354 Febrile convulsion
126123542 12612354 Hypoglycaemia
126123542 12612354 Nasopharyngitis

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126123542 12612354 1 20160714 0
126123542 12612354 3 20160714 0