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
125527631 12552763 1 I 20160621 20160627 20160713 20160713 EXP BR-PFIZER INC-2016321959 PFIZER 55.00 YR F Y 0.00000 20160713 CN BR BR

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
125527631 12552763 1 PS DOXYCYCLINE. DOXYCYCLINE 1 Oral 100 MG, 2X/DAY 1800 MG U 50457501A 50006 100 MG DISPERSIBLE TABLET BID
125527631 12552763 2 SS LEVOFLOXACIN. LEVOFLOXACIN 1 500 MG, UNK U 0 500 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125527631 12552763 1 Sinusitis
125527631 12552763 2 Sinusitis

Outcome of event

Event ID CASEID OUTC COD
125527631 12552763 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125527631 12552763 Abdominal pain
125527631 12552763 Back pain
125527631 12552763 Blood pressure increased
125527631 12552763 Cough decreased
125527631 12552763 Drug ineffective
125527631 12552763 Gastric disorder
125527631 12552763 Headache
125527631 12552763 Insomnia
125527631 12552763 Sluggishness
125527631 12552763 Spinal pain
125527631 12552763 Vomiting

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
125527631 12552763 1 20160621 20160629 0
125527631 12552763 2 2016 2016 0