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
126710241 12671024 1 I 20130124 0 20160819 20160819 DIR 66.00 YR F N 144.00000 LBS 0 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
126710241 12671024 1 PS CIPROFLOXACN CIPROFLOXACIN 1 Oral 20 PILLS 1 TAB 2X DAY MOUTH N D 0 1 DF COATED TABLET BID
126710241 12671024 2 SS AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 Oral 6 PILLS 2 TAB THEN 1 FOR 4 DAYS MOUTH 0 COATED TABLET
126710241 12671024 3 C ARMOUR THYROID THYROID, PORCINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126710241 12671024 1 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
126710241 12671024 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126710241 12671024 Anxiety
126710241 12671024 Dizziness
126710241 12671024 Dyspepsia
126710241 12671024 Fall
126710241 12671024 Feeling abnormal
126710241 12671024 Heart rate increased
126710241 12671024 Hyperacusis
126710241 12671024 Hypertension
126710241 12671024 Hypoaesthesia
126710241 12671024 Insomnia
126710241 12671024 Nausea
126710241 12671024 Neck pain
126710241 12671024 Oropharyngeal pain
126710241 12671024 Panic attack
126710241 12671024 Personality change
126710241 12671024 Vertigo

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

no results found

Therapies reported

no results found