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
127252101 12725210 1 I 20160813 0 20160905 20160905 DIR US-FDA-349805 FDA-CTU 25.00 YR F N 59.85000 KG 20160905 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
127252101 12725210 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral N D 0 1 DF COATED TABLET BID
127252101 12725210 2 C LAXATIVE UNSPECIFIED INGREDIENT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127252101 12725210 1 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
127252101 12725210 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127252101 12725210 Abdominal pain upper
127252101 12725210 Aptyalism
127252101 12725210 Blood phosphorus decreased
127252101 12725210 Chills
127252101 12725210 Constipation
127252101 12725210 Decreased appetite
127252101 12725210 Dry eye
127252101 12725210 Dry mouth
127252101 12725210 Eye swelling
127252101 12725210 Fatigue
127252101 12725210 Head discomfort
127252101 12725210 Headache
127252101 12725210 Hypersomnia
127252101 12725210 Impaired work ability
127252101 12725210 Nocturia
127252101 12725210 Pain
127252101 12725210 Peripheral swelling
127252101 12725210 Pyrexia
127252101 12725210 Rash papular
127252101 12725210 Rash pruritic
127252101 12725210 Skin exfoliation
127252101 12725210 Skin warm

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
127252101 12725210 1 20160812 0