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
126590761 12659076 1 I 20160809 20160817 20160817 EXP CA-ABBVIE-16P-028-1703605-00 ABBVIE 0.00 F Y 0.00000 20160817 CN CA CA

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
126590761 12659076 1 PS BIAXIN CLARITHROMYCIN 1 Unknown U UNKNOWN 50698

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126590761 12659076 1 Respiratory tract infection

Outcome of event

Event ID CASEID OUTC COD
126590761 12659076 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126590761 12659076 Anxiety
126590761 12659076 Asthenia
126590761 12659076 Chest discomfort
126590761 12659076 Dyspnoea
126590761 12659076 Feeling abnormal
126590761 12659076 Hallucination, auditory
126590761 12659076 Heart rate irregular
126590761 12659076 Palpitations
126590761 12659076 Sleep disorder
126590761 12659076 Toxicity to various agents
126590761 12659076 Vomiting

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

no results found

Therapies reported

no results found