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
126253251 12625325 1 I 20160418 20160725 20160805 20160805 EXP GB-MHRA-EYC 00142672 GB-TEVA-681001ACC TEVA 38.00 YR F Y 68.00000 KG 20160805 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
126253251 12625325 1 PS TOPIRAMATE. TOPIRAMATE 1 Oral 100 MILLIGRAM DAILY; 400 MG Y U 76317 50 MG BID
126253251 12625325 2 C IBUPROFEN. IBUPROFEN 1 0
126253251 12625325 3 C PARACETAMOL ACETAMINOPHEN 1 0
126253251 12625325 4 C SUMATRIPTAN. SUMATRIPTAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126253251 12625325 1 Cluster headache

Outcome of event

Event ID CASEID OUTC COD
126253251 12625325 DS
126253251 12625325 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126253251 12625325 Abulia
126253251 12625325 Anger
126253251 12625325 Anxiety
126253251 12625325 Blepharospasm
126253251 12625325 Cognitive disorder
126253251 12625325 Confusional state
126253251 12625325 Cough
126253251 12625325 Decreased appetite
126253251 12625325 Disturbance in attention
126253251 12625325 Dysgeusia
126253251 12625325 Eye pain
126253251 12625325 Fatigue
126253251 12625325 Feeling abnormal
126253251 12625325 Memory impairment
126253251 12625325 Mood swings
126253251 12625325 Paraesthesia
126253251 12625325 Tearfulness

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
126253251 12625325 1 20160414 20160525 0