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
125233021 12523302 1 I 20160531 20160702 20160702 PER US-ASTRAZENECA-2016SE58657 ASTRAZENECA 0.00 F Y 124.70000 KG 20160702 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
125233021 12523302 1 PS ARIMIDEX ANASTROZOLE 1 Oral UNKNOWN, DAILY 20541 TABLET
125233021 12523302 2 SS ATENOLOL. ATENOLOL 1 Unknown UNKNOWN 0
125233021 12523302 3 C WARFARIN WARFARIN 1 0
125233021 12523302 4 C LEVOTHYROXINE. LEVOTHYROXINE 1 DAILY 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125233021 12523302 1 Prophylaxis
125233021 12523302 2 Hypertension
125233021 12523302 3 Anticoagulant therapy
125233021 12523302 4 Thyroid disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125233021 12523302 Alopecia
125233021 12523302 Balance disorder
125233021 12523302 Hot flush
125233021 12523302 Hyperhidrosis
125233021 12523302 Insomnia
125233021 12523302 Memory impairment
125233021 12523302 Musculoskeletal stiffness
125233021 12523302 Pain
125233021 12523302 Somnolence
125233021 12523302 Trigger finger

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
125233021 12523302 1 201406 0