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
117201363 11720136 3 F 201306 20160822 20151110 20160824 EXP US-BAYER-2015-458931 BAYER 53.00 YR A F Y 59.86000 KG 20160825 MD 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
117201363 11720136 1 PS CIPRO CIPROFLOXACIN HYDROCHLORIDE 1 19537 TABLET
117201363 11720136 2 SS CIPROFLOXACIN. CIPROFLOXACIN 1 UNK 0
117201363 11720136 3 SS CIPROFLOXACIN. CIPROFLOXACIN 1 UNK 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
117201363 11720136 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117201363 11720136 Asthenia
117201363 11720136 Burning sensation
117201363 11720136 Depression
117201363 11720136 Disturbance in attention
117201363 11720136 Dizziness
117201363 11720136 Dysstasia
117201363 11720136 Emotional distress
117201363 11720136 Gait disturbance
117201363 11720136 Hypoaesthesia
117201363 11720136 Injury
117201363 11720136 Loss of employment
117201363 11720136 Neuropathy peripheral
117201363 11720136 Pain
117201363 11720136 Tremor

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
117201363 11720136 2 201304 0
117201363 11720136 3 201305 0