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
126809431 12680943 1 I 20160818 20160824 20160824 PER US-PFIZER INC-2016394747 PFIZER 57.00 YR F Y 0.00000 20160824 CN 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
126809431 12680943 1 PS RELPAX ELETRIPTAN HYDROBROMIDE 1 UNKNOWN U 21016 FILM-COATED TABLET
126809431 12680943 2 SS FROVA FROVATRIPTAN SUCCINATE 1 UNKNOWN U 0
126809431 12680943 3 SS MAXALT RIZATRIPTAN BENZOATE 1 UNKNOWN 0
126809431 12680943 4 SS AMERGE NARATRIPTAN HYDROCHLORIDE 1 UNKNOWN U 0
126809431 12680943 5 SS ZOMIG ZOLMITRIPTAN 1 UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126809431 12680943 1 Migraine
126809431 12680943 2 Migraine
126809431 12680943 3 Migraine
126809431 12680943 4 Migraine
126809431 12680943 5 Migraine

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126809431 12680943 Allergic sinusitis
126809431 12680943 Crying
126809431 12680943 Dehydration
126809431 12680943 Dizziness
126809431 12680943 Drug ineffective
126809431 12680943 Facial pain
126809431 12680943 Feeling abnormal
126809431 12680943 Headache
126809431 12680943 Immune system disorder
126809431 12680943 Impaired driving ability
126809431 12680943 Malaise
126809431 12680943 Mobility decreased
126809431 12680943 Muscle tightness
126809431 12680943 Pain
126809431 12680943 Parosmia
126809431 12680943 Swelling

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

no results found

Therapies reported

no results found