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
126178871 12617887 1 I 20111001 0 20160802 20160802 DIR 48.00 YR F N 185.00000 LBS 20160801 N 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
126178871 12617887 1 PS LEVAQUIN LEVOFLOXACIN 1 Oral Y D 0
126178871 12617887 2 C SINGULAIR MONTELUKAST SODIUM 1 0
126178871 12617887 3 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 0
126178871 12617887 4 C ALBUTERAL MDI 2 0
126178871 12617887 5 C BUSPAR BUSPIRONE HYDROCHLORIDE 1 0
126178871 12617887 6 C CELEXA CITALOPRAM HYDROBROMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126178871 12617887 1 Upper respiratory tract infection

Outcome of event

Event ID CASEID OUTC COD
126178871 12617887 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126178871 12617887 Arthralgia
126178871 12617887 Asthenia
126178871 12617887 Gait disturbance
126178871 12617887 Influenza like illness
126178871 12617887 Joint stiffness
126178871 12617887 Myalgia
126178871 12617887 Posturing
126178871 12617887 Serum sickness

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

no results found

Therapies reported

no results found