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
125707771 12570777 1 I 20151105 20151116 20160719 20160719 PER US-WATSON-2015-25167 WATSON 63.09 YR F Y 59.00000 KG 20160719 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
125707771 12570777 1 PS NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 Oral 1 TABLET, DAILY N UNKNOWN 40099 TABLET QD
125707771 12570777 2 SS AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 Oral 500 MG, DAILY UNKNOWN 0 500 MG QD
125707771 12570777 3 C DIPHENHYDRAMINE HYDROCHLORIDE. DIPHENHYDRAMINE HYDROCHLORIDE 1 25 MG, QHS 0 25 MG QD
125707771 12570777 4 C MUCINEX D GUAIFENESINPSEUDOEPHEDRINE HYDROCHLORIDE 1 Unknown 1 UNK, QAM UNKNOWN 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125707771 12570777 1 Pain
125707771 12570777 2 Preoperative care
125707771 12570777 3 Seasonal allergy
125707771 12570777 4 Seasonal allergy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125707771 12570777 Activities of daily living impaired
125707771 12570777 Dizziness
125707771 12570777 Headache
125707771 12570777 Nausea
125707771 12570777 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
125707771 12570777 1 20151105 20151109 0
125707771 12570777 2 20151105 0