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
127240701 12724070 1 I 20160722 0 20160904 20160904 DIR US-FDA-349786 FDA-CTU 50.00 YR F N 58.50000 KG 20160904 N 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
127240701 12724070 1 PS LEVOFLOXACIN. LEVOFLOXACIN 1 Oral N Y 20170609 0 1 DF COATED TABLET QD
127240701 12724070 3 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 0
127240701 12724070 5 C PRAVASTATIN. PRAVASTATIN 1 0
127240701 12724070 7 C MUCINEX D GUAIFENESINPSEUDOEPHEDRINE HYDROCHLORIDE 1 0
127240701 12724070 9 C FLONASE FLUTICASONE PROPIONATE 1 0
127240701 12724070 11 C MONTELUKAST MONTELUKAST SODIUM 1 0
127240701 12724070 13 C RIZATRIPTAN. RIZATRIPTAN 1 0
127240701 12724070 15 C ADVIL IBUPROFEN 1 0
127240701 12724070 17 C ALEVE NAPROXEN SODIUM 1 0
127240701 12724070 19 C MIGRAINE EXCEDRIN 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127240701 12724070 1 Sinusitis

Outcome of event

Event ID CASEID OUTC COD
127240701 12724070 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127240701 12724070 Arthralgia
127240701 12724070 Insomnia
127240701 12724070 Migraine
127240701 12724070 Pain
127240701 12724070 Tendon pain

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
127240701 12724070 1 20160609 20160708 0