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Index of reports
> All cases (96)
Below is the selection of adverse event reports related to Cipro (Ciprofloxacin) that includes all cases.
Reports 1 - 25 of 96 Next >>
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 65 year old female receiving Cipro (Ciprofloxacin)
Reported by a health professional (non-physician/pharmacist) from Canada on 2007-10-29
Patient: 65 year old female
Adverse reactions / side effects: Metastasis, Myocardial Infarction
Suspect drug(s):
Champix (Varenicline)
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Cipro
Dosage: unit dose: 500 mg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Altace; Hydrochlorothiazide; Lipitor; Metformin; Norvasc; Plavix
Adverse event in 71 year old female receiving Cipro (Ciprofloxacin)
Reported by a consumer/non-health professional from United States on 2007-10-25
Patient: 71 year old female, weighing 59.9 kg (131.8 pounds)
Adverse reactions / side effects: Hypertensive Encephalopathy, Blood Pressure Increased, Gastrointestinal Toxicity, Sensation of Heaviness, Anaemia, Chills, Hypotension, Rash, Small Intestinal Obstruction, Vision Blurred, Gastrointestinal Oedema, Acute Prerenal Failure, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Antidiarrhoeal NOS
Start date: 2007-02-01
Cipro
Indication: Drug USE FOR Unknown Indication
Contrast DYE
Xeloda
Administration route: Oral
Start date: 2007-02-08
End date: 2007-02-22
Xeloda
Administration route: Oral
Start date: 2007-02-23
End date: 2007-02-24
Other drugs received by patient: Altace; Atenolol
Adverse event in 36 year old female receiving Cipro (Ciprofloxacin)
Reported by a individual with unspecified qualification from United States on 2007-10-12
Patient: 36 year old female, weighing 42.6 kg (93.8 pounds)
Adverse reactions / side effects: Palpitations, Paraesthesia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Cipro (Ciprofloxacin)
Adverse event in female receiving Cipro (Ciprofloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-12
Patient: female, weighing 70.3 kg (154.7 pounds)
Adverse reactions / side effects: Hallucination
Suspect drug(s):
Cipro (Ciprofloxacin)
Adverse event in 3 year old male receiving Cipro (Ciprofloxacin)
Reported by a consumer/non-health professional from Canada on 2007-10-08
Patient: 3 year old male
Adverse reactions / side effects: Arthralgia, Pyrexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Cipro (Ciprofloxacin)
Adverse event in 22 year old female receiving Cipro (Ciprofloxacin)
Reported by a consumer/non-health professional from United States on 2007-10-08
Patient: 22 year old female
Adverse reactions / side effects: Renal Failure
Adverse event resulted in: hospitalization
Suspect drug(s):
Cipro
Indication: Urinary Tract Infection
Levaquin
Indication: Drug USE FOR Unknown Indication
Adverse event in 57 year old female receiving Cipro (Ciprofloxacin)
Reported by a consumer/non-health professional from United States on 2007-10-05
Patient: 57 year old female
Adverse reactions / side effects: Abdominal Pain Lower, Weight Decreased, Hypersensitivity, Steatorrhoea, Drug Ineffective, Diverticulitis, Drug Hypersensitivity, Flatulence, Abdominal Tenderness, Weight Increased, Anorexia, Weight Fluctuation, Rectal Discharge
Adverse event resulted in: hospitalization
Suspect drug(s):
Alli
Dosage: 3cap per day
Administration route: Oral
Indication: Weight Loss Diet
Start date: 2007-06-25
End date: 2007-09-01
Cipro
Indication: Diverticulitis
Start date: 2007-09-01
End date: 2007-09-01
Other drugs received by patient: Toprol-XL; Omeprazole; Vitamins; Ascorbic Acid; Calcium + Vitamin D; ONE A DAY Vitamin; Aspirin
Adverse event in female receiving Cipro (Ciprofloxacin)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-03
Patient: female, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Mouth Ulceration, Tongue Ulceration
Adverse event resulted in: hospitalization
Suspect drug(s):
Cipro
End date: 2007-09-21
Tygacil
Indication: Osteomyelitis
Start date: 2007-09-10
Other drugs received by patient: Paracetamol; Loratadine; Ranitidine; Caspofungin Acetate
Adverse event in 71 year old female receiving Cipro (Ciprofloxacin)
Reported by a consumer/non-health professional from United States on 2007-10-02
Patient: 71 year old female
Adverse reactions / side effects: Blood Pressure Increased, Hypertensive Encephalopathy, Sensation of Heaviness, Intestinal Obstruction, Rash, Convulsion, Visual Disturbance, Peritoneal Adhesions Division, Colitis, Gastrointestinal Oedema, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Antidiarrhoeal NOS
Start date: 2007-02-01
Cipro
Indication: Drug USE FOR Unknown Indication
Contrast DYE
Xeloda
Start date: 2007-02-13
End date: 2007-02-01
Other drugs received by patient: Altace; Atenolol
Adverse event in male receiving Cipro (Ciprofloxacin)
Reported by a individual with unspecified qualification from United States on 2007-10-01
Patient: male
Adverse reactions / side effects: Burning Sensation, LIP Swelling, Hypersensitivity, Dyspnoea, Face Oedema, Drug Interaction, Oxygen Saturation Decreased
Suspect drug(s):
Cipro (Ciprofloxacin)
Adverse event in 42 year old male receiving Cipro (Ciprofloxacin)
Reported by a individual with unspecified qualification from United States on 2007-10-01
Patient: 42 year old male
Adverse reactions / side effects: Pancreatitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Cipro (Ciprofloxacin)
Other drugs received by patient: Blood Pressure Medication
Adverse event in 58 year old female receiving Cipro (Ciprofloxacin)
Reported by a individual with unspecified qualification from United States on 2007-10-01
Patient: 58 year old female
Adverse reactions / side effects: Anaphylactic Shock, Throat Tightness
Suspect drug(s):
Cipro (Ciprofloxacin)
Other drugs received by patient: Avonex
Adverse event in 62 year old female receiving Cipro (Ciprofloxacin)
Reported by a individual with unspecified qualification from United States on 2007-10-01
Patient: 62 year old female
Adverse reactions / side effects: Tinnitus, Deafness, Hearing Impaired
Suspect drug(s):
Cipro
Dosage: 500 mg, bid, oral; bid, oral; 500 mg, bid, oral; bid, oral
Administration route: Oral
Indication: Cystitis Interstitial
Start date: 1995-06-22
Cipro
Dosage: 500 mg, bid, oral; bid, oral; 500 mg, bid, oral; bid, oral
Administration route: Oral
Indication: Cystitis Noninfective
Start date: 1995-06-22
Cipro
Dosage: 500 mg, bid, oral; bid, oral; 500 mg, bid, oral; bid, oral
Administration route: Oral
Indication: Dysuria
Start date: 1995-06-22
Cipro
Dosage: 500 mg, bid, oral; bid, oral; 500 mg, bid, oral; bid, oral
Administration route: Oral
Indication: Cystitis Interstitial
Start date: 1996-03-21
Cipro
Dosage: 500 mg, bid, oral; bid, oral; 500 mg, bid, oral; bid, oral
Administration route: Oral
Indication: Cystitis Noninfective
Start date: 1996-03-21
Cipro
Dosage: 500 mg, bid, oral; bid, oral; 500 mg, bid, oral; bid, oral
Administration route: Oral
Indication: Dysuria
Start date: 1996-03-21
Cipro
Dosage: 500 mg, bid, oral; bid, oral; 500 mg, bid, oral; bid, oral
Administration route: Oral
Indication: Cystitis Interstitial
Start date: 1996-08-01
Cipro
Dosage: 500 mg, bid, oral; bid, oral; 500 mg, bid, oral; bid, oral
Administration route: Oral
Indication: Cystitis Noninfective
Start date: 1996-08-01
Cipro
Dosage: 500 mg, bid, oral; bid, oral; 500 mg, bid, oral; bid, oral
Administration route: Oral
Indication: Dysuria
Start date: 1996-08-01
Cipro
Dosage: 500 mg, bid, oral; bid, oral; 500 mg, bid, oral; bid, oral
Administration route: Oral
Indication: Cystitis Interstitial
Start date: 1996-10-21
Cipro
Dosage: 500 mg, bid, oral; bid, oral; 500 mg, bid, oral; bid, oral
Administration route: Oral
Indication: Cystitis Noninfective
Start date: 1996-10-21
Cipro
Dosage: 500 mg, bid, oral; bid, oral; 500 mg, bid, oral; bid, oral
Administration route: Oral
Indication: Dysuria
Start date: 1996-10-21
Adverse event in 38 year old male receiving Cipro (Ciprofloxacin)
Reported by a individual with unspecified qualification from United States on 2007-10-01
Patient: 38 year old male
Adverse reactions / side effects: Diarrhoea, Clostridial Infection
Suspect drug(s):
Cipro
Dosage: oral
Administration route: Oral
Indication: Infection Prophylaxis
Cipro
Dosage: oral
Administration route: Oral
Indication: Prostate Infection
Adverse event in 66 year old female receiving Cipro (Ciprofloxacin)
Reported by a individual with unspecified qualification from United States on 2007-10-01
Patient: 66 year old female
Adverse reactions / side effects: Pain in Extremity, Tendon Rupture, Abasia, Oedema Peripheral
Suspect drug(s):
Cipro
Dosage: 500 mg, total daily, oral; 750 mg, total daily, oral
Administration route: Oral
Indication: Bronchitis
Cipro
Dosage: 500 mg, total daily, oral; 750 mg, total daily, oral
Administration route: Oral
Indication: Bronchitis
Other drugs received by patient: Cholesterol Medication; Budesonide
Adverse event in male receiving Cipro (Ciprofloxacin)
Reported by a physician from United States on 2007-10-01
Patient: male
Adverse reactions / side effects: Jaundice Cholestatic
Suspect drug(s):
Cipro (Ciprofloxacin)
Adverse event in 45 year old female receiving Cipro (Ciprofloxacin)
Reported by a individual with unspecified qualification from United States on 2007-10-01
Patient: 45 year old female, weighing 77.1 kg (169.6 pounds)
Adverse reactions / side effects: Abdominal Pain, Fatigue, Nausea, Haemorrhoids, Anger, Clostridium Difficile Colitis
Suspect drug(s):
Cipro
Dosage: 500 mg, total daily, oral
Administration route: Oral
Indication: Diverticulitis
Start date: 2007-01-28
Metronidazole
Indication: Diverticulitis
Adverse event in male receiving Cipro (Ciprofloxacin)
Reported by a physician from United States on 2007-10-01
Patient: male
Adverse reactions / side effects: Tinnitus, Tendonitis, Tremor
Suspect drug(s):
Cipro (Ciprofloxacin)
Adverse event in receiving Cipro (Ciprofloxacin)
Reported by a individual with unspecified qualification from United States on 2007-10-01
Patient:
Adverse reactions / side effects: Hypersensitivity
Adverse event resulted in: hospitalization
Suspect drug(s):
Cipro (Ciprofloxacin)
Adverse event in 51 year old male receiving Cipro (Ciprofloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-01
Patient: 51 year old male, weighing 84.4 kg (185.6 pounds)
Adverse reactions / side effects: Platelet Count Decreased
Suspect drug(s):
Agrylin
Dosage: 0.5 mg, qid, oral
Indication: Polycythaemia Vera
Start date: 2003-05-06
End date: 2007-02-06
Agrylin
Dosage: 0.5 mg, qid, oral
Indication: Polycythaemia Vera
Start date: 2007-02-16
Cipro
Indication: Drug USE FOR Unknown Indication
Adverse event in 68 year old male receiving Cipro (Ciprofloxacin)
Reported by a individual with unspecified qualification from United States on 2007-10-01
Patient: 68 year old male
Adverse reactions / side effects: Pancreatitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Cipro (Ciprofloxacin)
Other drugs received by patient: Blood Pressure Medication
Adverse event in male receiving Cipro (Ciprofloxacin)
Reported by a individual with unspecified qualification from United States on 2007-07-31
Patient: male
Adverse reactions / side effects: Rash
Suspect drug(s):
Cipro (Ciprofloxacin)
Other drugs received by patient: Calcitriol; Docusate; Clindamycin HCL
Adverse event in receiving Cipro (Ciprofloxacin)
Reported by a physician from United States on 2007-07-30
Patient:
Adverse reactions / side effects: Torsade DE Pointes
Suspect drug(s):
Avelox
Indication: Drug USE FOR Unknown Indication
Cipro
Indication: Drug USE FOR Unknown Indication
Adverse event in receiving Cipro (Ciprofloxacin)
Reported by a physician from United States on 2007-07-30
Patient:
Adverse reactions / side effects: Torsade DE Pointes
Adverse event resulted in: death
Suspect drug(s):
Avelox
Indication: Drug USE FOR Unknown Indication
Cipro
Indication: Drug USE FOR Unknown Indication
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