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
118303684 11830368 4 F 20160629 20151214 20160714 EXP US-JNJFOC-20151121815 JANSSEN GOLOMB BA, KOSLIK HJ, REDD AJ. FLUOROQUINOLONE-INDUCED SERIOUS, PERSISTENT, MULTISYMPTOM ADVERSE EFFECTS. BRITISH MEDICAL JOURNAL CASE REPORTS 2015;2015. 55.00 YR A F Y 0.00000 20160714 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
118303684 11830368 1 SS LEVOFLOXACIN. LEVOFLOXACIN 1 Unknown U U 0 UNSPECIFIED
118303684 11830368 2 SS LEVOFLOXACIN. LEVOFLOXACIN 1 Unknown 10 DAYS U U 0 500 MG UNSPECIFIED QD
118303684 11830368 3 SS LEVOFLOXACIN. LEVOFLOXACIN 1 Unknown 5 DAYS U U 0 750 MG UNSPECIFIED
118303684 11830368 4 SS LEVOFLOXACIN. LEVOFLOXACIN 1 Unknown U U 0 UNSPECIFIED
118303684 11830368 5 SS LEVOFLOXACIN. LEVOFLOXACIN 1 Unknown 5 DAYS U U 0 750 MG UNSPECIFIED
118303684 11830368 6 SS LEVOFLOXACIN. LEVOFLOXACIN 1 Unknown U U 0 UNSPECIFIED
118303684 11830368 7 SS LEVOFLOXACIN. LEVOFLOXACIN 1 Unknown 10 DAYS U U 0 500 MG UNSPECIFIED QD
118303684 11830368 8 PS LEVOFLOXACIN. LEVOFLOXACIN 1 Unknown U U 20634 UNSPECIFIED
118303684 11830368 9 C ALENDRONATE ALENDRONATE SODIUM 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118303684 11830368 1 Urinary tract infection
118303684 11830368 2 Urinary tract infection
118303684 11830368 3 Urinary tract infection
118303684 11830368 4 Urinary tract infection
118303684 11830368 5 Sinusitis
118303684 11830368 6 Sinusitis
118303684 11830368 7 Sinusitis
118303684 11830368 8 Sinusitis
118303684 11830368 9 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
118303684 11830368 DS
118303684 11830368 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118303684 11830368 Affective disorder
118303684 11830368 Alopecia
118303684 11830368 Amnesia
118303684 11830368 Anxiety
118303684 11830368 Arthralgia
118303684 11830368 Chondropathy
118303684 11830368 Cognitive disorder
118303684 11830368 Confusional state
118303684 11830368 Disturbance in attention
118303684 11830368 Fatigue
118303684 11830368 Headache
118303684 11830368 Mental disorder
118303684 11830368 Muscular weakness
118303684 11830368 Myalgia
118303684 11830368 Nervous system disorder
118303684 11830368 Neuropathy peripheral
118303684 11830368 Pain
118303684 11830368 Psychiatric symptom
118303684 11830368 Respiratory muscle weakness
118303684 11830368 Sensory disturbance
118303684 11830368 Sleep disorder
118303684 11830368 Somnolence
118303684 11830368 Tendon disorder
118303684 11830368 Tendonitis
118303684 11830368 Tinnitus
118303684 11830368 Toxicity to various agents
118303684 11830368 Visual impairment

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

no results found

Therapies reported

no results found