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Index of reports
> Cases resulting in hospitalization (42)
> Cases with Intestinal Obstruction (5)
Below is the selection of adverse event reports related to Cipro (Ciprofloxacin) that includes cases resulting in hospitalization where reactions include intestinal obstruction.
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 92 year old female receiving Cipro (Ciprofloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-21
Patient: 92 year old female
Adverse reactions / side effects: Vomiting, Intestinal Obstruction, Abdominal Pain Upper
Adverse event resulted in: hospitalization
Suspect drug(s):
Cipro (Ciprofloxacin)
Other drugs received by patient: Vasotec; Clonidine; Hydrochlorothiazide; Iron; Calcium Chloride
Adverse event in male receiving Cipro (Ciprofloxacin)
Reported by a physician from United States on 2007-04-27
Patient: male, weighing 69.0 kg (151.8 pounds)
Adverse reactions / side effects: Angina Pectoris, Blood Chloride Decreased, Platelet Count Increased, Intestinal Obstruction, Constipation, Haemoglobin Decreased, Haematocrit Decreased, RED Blood Cell Count Decreased, Blood Sodium Decreased, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Acetylsalicylic Acid SRT
Administration route: Oral
Indication: Prophylaxis
Start date: 1986-01-01
End date: 2003-08-10
Amiodarone HCL
Administration route: Oral
Cipro
Indication: Prophylaxis
Fluorouracil
Dosage: 500 mg/m*2, day 1 and 8 cycle
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-11
Fluorouracil
Dosage: 500 mg/m*2, day 1 and 8 cycle
Start date: 2003-08-18
End date: 2003-08-18
Irinotecan HCL
Dosage: 125 mg/m*2, day 1 and 8, cycle
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-11
Irinotecan HCL
Dosage: 125 mg/m*2, day 1 and 8, cycle
Start date: 2003-08-18
End date: 2003-08-18
Leucovorin Calcium
Dosage: ^(20 mg/m*2, cycle 1, day 1 and^
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Protonix
Administration route: Oral
Toprol-XL
Administration route: Oral
Indication: Hypertension
Xanax
Administration route: Oral
Indication: Sleep Disorder
Zetia
Administration route: Oral
Indication: Hypercholesterolaemia
Adverse event in 57 year old male receiving Cipro (Ciprofloxacin)
Reported by a individual with unspecified qualification from United States on 2007-04-26
Patient: 57 year old male
Adverse reactions / side effects: Haemoglobin Decreased, Abdominal Pain, Haematocrit Decreased, Angina Pectoris, Intestinal Obstruction, Constipation, Blood Sodium Decreased, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Amiodarone HCL
Dosage: 200mg/bid/po
Administration route: Oral
Aspirin
Dosage: 81 mg/daily
Indication: Prophylaxis
Start date: 1986-01-01
End date: 2003-08-10
Cipro
Dosage: 250 mg/daily
Indication: Prophylaxis
Protonix
Dosage: 40 mg/daily/po
Administration route: Oral
Indication: Hypertension
Toprol-XL
Dosage: 50 mg/daily/po
Administration route: Oral
Indication: Hypertension
Xanax
Dosage: 0.5 mg/daily/po
Administration route: Oral
Indication: Sleep Disorder
Zetia
Dosage: 10 mg/daily/po
Administration route: Oral
Indication: Blood Cholesterol
Other drugs received by patient: Fluorouracil; Irinotecan HCL; Leucovorin Calcium
Adverse event in 92 year old female receiving Cipro (Ciprofloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-23
Patient: 92 year old female
Adverse reactions / side effects: Vomiting, Intestinal Obstruction, Abdominal Pain Upper
Adverse event resulted in: hospitalization
Suspect drug(s):
Cipro (Ciprofloxacin)
Other drugs received by patient: Vasotec; Clonidine; Hydrochlorothiazide; Iron; Calcium
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