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
126632521 12663252 1 I 20140101 20160812 20160818 20160818 EXP GB-MHRA-EYC 00143537 GB-GLENMARK GENERICS (EUROPE) LTD.-2016GMK023974 GLENMARK 0.00 Y 0.00000 20160818 CN GB GB

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
126632521 12663252 1 PS TOPIRAMATE. TOPIRAMATE 1 Oral UNK Y 77627
126632521 12663252 2 C AMITRIPTYLINE AMITRIPTYLINE 1 Unknown UNK 0
126632521 12663252 3 C STEROIDS UNSPECIFIED INGREDIENT 1 Nasal UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126632521 12663252 1 Hemiplegic migraine
126632521 12663252 2 Product used for unknown indication
126632521 12663252 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126632521 12663252 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126632521 12663252 Abdominal pain upper
126632521 12663252 Decreased appetite
126632521 12663252 Food intolerance
126632521 12663252 Lethargy
126632521 12663252 Palpitations
126632521 12663252 Product use issue

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
126632521 12663252 1 20130301 20140401 0