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Index of reports
> Cases resulting in disability (6)
Below is the selection of adverse event reports related to Cipro (Ciprofloxacin) that includes cases resulting in disability.
Adverse event in male receiving Cipro (Ciprofloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-31
Patient: male, weighing 108.9 kg (239.5 pounds)
Adverse reactions / side effects: Tendon Rupture, Injury
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Cipro
Dosage: 500mg bid po x 7 days
Administration route: Oral
Indication: Prostatomegaly
Start date: 1999-08-01
Cipro
Dosage: 500mg bid po x 7 days
Administration route: Oral
Indication: Urinary Tract Infection
Start date: 1999-08-01
Cipro
Dosage: 500mg bid po x 21 days
Administration route: Oral
Indication: Prostatitis
Start date: 2001-03-01
Cipro
Dosage: 500 bid x 21 days
Indication: Prostatitis
Start date: 1999-08-12
Septra
Dosage: bid
Start date: 1999-07-20
End date: 1999-07-29
Adverse event in male receiving Cipro (Ciprofloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-08
Patient: male
Adverse reactions / side effects: Neuropathy, Nerve Injury, Nausea, Tremor, Myalgia, Arthralgia, Balance Disorder, Insomnia, Swelling, Feeling Abnormal
Adverse event resulted in: disablity
Suspect drug(s):
Cipro (Ciprofloxacin)
Adverse event in 21 year old male receiving Cipro (Ciprofloxacin)
Reported by a physician from United Kingdom on 2007-03-30
Patient: 21 year old male
Adverse reactions / side effects: Arthralgia, C-Reactive Protein Increased, Joint Swelling, RED Blood Cell Sedimentation Rate Increased, Joint Stiffness
Adverse event resulted in: disablity
Suspect drug(s):
Cipro (Ciprofloxacin)
Adverse event in 57 year old female receiving Cipro (Ciprofloxacin)
Reported by a consumer/non-health professional from United States on 2007-03-20
Patient: 57 year old female, weighing 126.6 kg (278.4 pounds)
Adverse reactions / side effects: Stomatitis, Nail Discolouration, Wound, Drug Hypersensitivity, Malnutrition, Erythrodermic Psoriasis, Nail Hypertrophy, Onychomadesis, Renal Failure, Bacteria Blood Identified, Dehydration, Alopecia, Blood Pressure Decreased, Shock Hypoglycaemic, Infection
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Cipro
Vancomycin HCL
Dosage: n/a
Indication: Arthritis Infective
Start date: 2005-08-30
End date: 2005-09-24
Vancomycin HCL
Dosage: n/a
Indication: Post Procedural Infection
Start date: 2005-08-30
End date: 2005-09-24
Adverse event in female receiving Cipro (Ciprofloxacin)
Reported by a consumer/non-health professional from United States on 2007-01-29
Patient: female
Adverse reactions / side effects: Pain in Extremity, Neuralgia
Adverse event resulted in: disablity
Suspect drug(s):
Cipro (Ciprofloxacin)
Adverse event in male receiving Cipro (Ciprofloxacin)
Reported by a physician from United States on 2007-01-10
Patient: male, weighing 110.2 kg (242.5 pounds)
Adverse reactions / side effects: Tendon Pain, Fatigue, Arthralgia, Pain in Extremity, Disease Progression
Adverse event resulted in: disablity
Suspect drug(s):
Cipro (Ciprofloxacin)
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