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
126740191 12674019 1 I 20140101 20160812 20160822 20160822 EXP GB-MHRA-EYC 00143537 GB-MYLANLABS-2016M1034100 MYLAN 0.00 Y 0.00000 20160822 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
126740191 12674019 1 PS TOPIRAMATE. TOPIRAMATE 1 Oral NOT KNOWN Y U 76314
126740191 12674019 2 C AMITRIPTYLINE AMITRIPTYLINE 1 UNK U 0
126740191 12674019 3 C STEROIDS UNSPECIFIED INGREDIENT 1 Nasal UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126740191 12674019 1 Hemiplegic migraine

Outcome of event

Event ID CASEID OUTC COD
126740191 12674019 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126740191 12674019 Abdominal pain upper
126740191 12674019 Decreased appetite
126740191 12674019 Food intolerance
126740191 12674019 Lethargy
126740191 12674019 Palpitations

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
126740191 12674019 1 20130301 20140401 0