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
125777511 12577751 1 I 20160712 20160721 20160721 PER US-ASTRAZENECA-2016SE75962 ASTRAZENECA 0.00 F Y 0.00000 20160721 OT US US

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
125777511 12577751 1 PS ZOMIG ZOLMITRIPTAN 1 Oral U 20768 TABLET
125777511 12577751 2 SS ZOMIG ZOLMITRIPTAN 1 Oral ZOLMITRIPTAN U 20768 TABLET

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125777511 12577751 Headache
125777511 12577751 Malaise

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

no results found

Therapies reported

no results found