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
125997171 12599717 1 I 20160414 20160727 20160727 PER US-SA-2016SA081671 AVENTIS 51.00 YR A F Y 0.00000 20160727 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
125997171 12599717 1 PS AMBIEN ZOLPIDEM TARTRATE 1 Oral U UNKNOWN 19908 FILM-COATED TABLET
125997171 12599717 2 SS JAKAFI RUXOLITINIB 1 Unknown U UNKNOWN 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125997171 12599717 Anxiety
125997171 12599717 Chest pain
125997171 12599717 Contusion
125997171 12599717 Dizziness
125997171 12599717 Eye pain
125997171 12599717 Feeling abnormal
125997171 12599717 Headache
125997171 12599717 Insomnia
125997171 12599717 Migraine
125997171 12599717 Somnolence
125997171 12599717 Tinnitus

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

no results found

Therapies reported

no results found