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
125317271 12531727 1 I 20160624 20160706 20160706 PER US-BAYER-2016-130244 BAYER 0.00 F Y 0.00000 20160706 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
125317271 12531727 1 PS CIPRO CIPROFLOXACIN HYDROCHLORIDE 1 UNK 19537 TABLET
125317271 12531727 2 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 UNK 0 FILM-COATED TABLET
125317271 12531727 3 SS LEVAQUIN LEVOFLOXACIN 1 UNK 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125317271 12531727 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125317271 12531727 Asthenia
125317271 12531727 Burning sensation
125317271 12531727 Cardiovascular disorder
125317271 12531727 Hypoaesthesia
125317271 12531727 Mental disorder
125317271 12531727 Musculoskeletal disorder
125317271 12531727 Nervous system disorder
125317271 12531727 Neurological symptom
125317271 12531727 Neuropathy peripheral
125317271 12531727 Pain
125317271 12531727 Paraesthesia
125317271 12531727 Skin disorder

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

no results found

Therapies reported

no results found