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Ciproflaxacin Side Effects submitted to FDA
Total Ciproflaxacin reports: 3.Ciproflaxacin FDA safety alerts: No.
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FDA Reported Ciproflaxacin Side Effects: international normalised ratio increased, coagulopathy, activated partial thromboplastin time prolonged, oliguria, nephropathy, incorrect dose administered, crystal urine present, blood creatinine increased, tendon rupture, diabetes insipidus, creatine urine increased,
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Ciproflaxacin Side Effects Report #5446122-8
Consumer or non-health professional from UNITED KINGDOM reported CIPROFLAXACIN problem on Aug 14, 2007. Female patient, 29 years of age, was treated with CIPROFLAXACIN. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, coagulopathy, international normalised ratio increased. CIPROFLAXACIN dosage: 800 MG (400 MG, 2 IN 1 D);. During the same period patient was treated with TOBRAMYCIN. Patient recovered.
Ciproflaxacin Side Effects Report #5347127-8
CIPROFLAXACIN problem was reported by a Physician from UNITED STATES on Apr 25, 2007. Female patient, 90 years of age, was diagnosed with proteus infection and was treated with CIPROFLAXACIN. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, crystal urine present, incorrect dose administered, nephropathy, oliguria. CIPROFLAXACIN dosage: 1500,00 MG. Patient recovered.
Ciproflaxacin Side Effects Report #5292002-0
Health Professional from UNITED STATES reported CIPROFLAXACIN problem on Apr 06, 2007. Male patient, weighting 160.0 lb, was diagnosed with pharyngolaryngeal pain and was treated with CIPROFLAXACIN. After drug was administered, patient experienced the following problems/side effects: tendon rupture. CIPROFLAXACIN dosage: 500MG BID PO. Patient recovered.
Ciproflaxacin Side Effects


