Cipro I.V. Side Effects

Generic Name: ciprofloxacin,ciprofloxacin hydrochloride

Please note - some side effects for Cipro I.V. may not be reported. Always consult your doctor or healthcare specialist for medical advice. You may also report side effects to the FDA.

Side Effects of Cipro I.V. - for the Consumer

Cipro I.V.

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome when using Cipro I.V.:

Diarrhea; dizziness; headache; loss of appetite; nausea; stomach upset; vomiting.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or tarry stools; burning, numbness, tingling, pain, or weakness of the arms, hands, legs, or feet; chest pain; dark urine or unusual change in the amount of urine; fainting; fever, chills, or unusual cough; hallucinations; inability to move or bear weight on a joint or tendon area; irregular heartbeat; loss of consciousness; moderate to severe sunburn; mood or mental changes (eg, new or worsening anxiety, agitation, confusion, depression, restlessness, sleeplessness); muscle pain or weakness; pain, soreness, redness, swelling, weakness, or bruising of a tendon or joint area; pale stools; persistent sore throat; red, swollen, blistered, or peeling skin; seizures; severe or persistent diarrhea; severe or persistent dizziness; shortness of breath or trouble breathing; stomach cramps or pain; suicidal thoughts or actions; tremors; unusual bruising or bleeding; unusual fatigue; vaginal yeast infection; vision changes; yellowing of the skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

Side Effects by Body System - for Healthcare Professionals

General

In clinical trials, oral ciprofloxacin was most frequently associated with nausea (5.2%), diarrhea (2.3%), vomiting (2%), abdominal pain or discomfort (1.7%), headache (1.2%), restlessness (1.1%), and rash (1.1%). Most side effects were described as mild to moderate; 3.5% of patients discontinued treatment due to side effects. Intravenous ciprofloxacin was most frequently associated with nausea, diarrhea, central nervous system disturbance, infusion site reactions, hepatic enzyme abnormalities, eosinophilia, headache, restlessness, and rash. The majority of these effects were of mild to moderate severity.

Of the individuals (n=3428) taking oral ciprofloxacin for anthrax prophylaxis, side effects included severe nausea, vomiting, diarrhea, or abdominal pain (19%); fainting, lightheadedness, or dizziness (14%); heartburn or acid reflux (7%); rash, hives, or itchy skin (6%). Three percent discontinued it due to adverse events.

Gastrointestinal

The onset of pseudomembranous colitis symptoms may occur during or after antimicrobial treatment.

Nineteen percent of the individuals (n=3428) taking oral ciprofloxacin for anthrax prophylaxis reported severe nausea, vomiting, diarrhea, or abdominal pain, and 7% reported heartburn or acid reflux.

Extended-release ciprofloxacin (Proquin XR) reportedly has been associated with a lower incidence of gastrointestinal side effects.

Gastrointestinal side effects have included nausea, diarrhea, vomiting, heartburn, and acid reflux. Abdominal pain or discomfort, anorexia, Clostridium difficile-associated diarrhea, constipation, dyspepsia, dysphagia, flatulence, gastrointestinal bleeding, ileus, intestinal perforation, mouth dryness, oral and gastrointestinal moniliasis, mouth dryness, oral candidiasis, oral ulceration, painful oral mucosa, pancreatitis, aggravated irritable bowel syndrome, lower abdominal pain, and pseudomembranous colitis have been reported in up to 1% of patients.

Dermatologic

Dermatologic side effects have included rash (1%), and pruritus, urticaria, cutaneous candidiasis, flushing, increased perspiration, photosensitivity/phototoxicity reaction, and hyperpigmentation (less than 1%). Sweating has been reported. At least one case of photoinduced acute exanthematous pustulosis has been reported.

Six percent of the individuals (n=3428) taking ciprofloxacin for anthrax prophylaxis reported rashes, hives, or itchy skin.

Nervous system

Nervous system side effects have included abnormal gait, anorexia, ataxia, convulsive seizures, dizziness, drowsiness, dysphasia, grand mal convulsion, headache, insomnia, irritability, lethargy, lightheadedness, malaise, myasthenia gravis, paresthesia, restlessness, syncope, tremor, unresponsiveness, weakness, and disturbance in attention in less than 1% of patients. Agitation, benign intracranial hypertension, confusion, dysesthesia, dyskinesia, hyperesthesia, hypoesthesia, tinnitus, hearing loss, bad taste, taste loss, anosmia, migraine, neuropathy, paresis, peripheral neuropathy, polyneuropathy, exacerbation of myasthenia gravis, twitching, and aseptic meningitis have also been reported.

One survey reported 11 cases of peripheral neuropathy associated with ciprofloxacin. The severity ranged from mild and reversible to severe and persistent. In one case, a 44-year-old female developed numbness, allodynia, hypesthesia, tremors, electrical and diffuse burning sensations, twitching, disorientation, visual impairment, nausea, temperature intolerance, rash, and palpitations, and remained disabled after 29 months.

Seizures have been reported in 2 patients given ciprofloxacin and foscarnet. The temporal association between the onset of seizures and drug administration suggests a possible drug interaction, although a causal relationship could not be established in either case. Ciprofloxacin and foscarnet are individually epileptogenic, and their concurrent use may potentiate the risk of seizures.

Fourteen percent of the individuals (n=3428) taking ciprofloxacin for anthrax prophylaxis reported fainting, lightheadedness, or dizziness.

Hypersensitivity

At least two cases have been reported of patients developing a cutaneous vasculitis related to ciprofloxacin use. The vasculitis resolved without medical intervention following discontinuation of the drug.

Photosensitivity is seen most frequently when patients are exposed to intense sun, as for example when used for the treatment or prophylaxis of traveler's diarrhea.

A 27-year-old woman with mild systemic erythematosus developed toxic epidermal necrolysis (TEN) after starting a second course of oral ciprofloxacin following a previous 5-day course. She developed a rash, high fever, and diarrhea after taking the second dose and presented with diffuse rash, epidermal sloughing of 60% of the skin, desquamation of the lips, shock, and respiratory distress. She died on the twenty-eighth hospital day of TEN, right ventricular failure, and acute respiratory distress syndrome. As of 2003, 9 cases of TEN, including 5 fatalities, have been reported in the literature.

Hypersensitivity side effects have included anaphylaxis (including life-threatening anaphylactic shock), bullous pemphigoid, erythema multiforme, Stevens-Johnson syndrome, exfoliative dermatitis, fixed eruption, toxic epidermal necrolysis (Lyell's syndrome), vasculitis, angioedema, edema of the lips, face, neck, conjunctivae, hands or lower extremities, purpura, fever, chills, flushing, pruritus, urticaria, vesicles, erythema nodosum, photosensitivity/phototoxicity reaction, allergic interstitial nephritis, lobular panniculitis, anaphylactoid reactions, necrotizing vasculitis, serum sickness-like reaction, and cutaneous vasculitis. Anaphylactic reactions may occur at an increased incidence among HIV-infected individuals.

Local

Local side effects have included injection site irritation and induration with intravenous infusion over less than 30 minutes or when a small vein in the back of the hand is used. The manufacturer recommends an infusion time of 1 hour. Thrombophlebitis, burning, pain, pruritus, paresthesia, erythema and swelling of the infusion site have been reported in less than 1% of patients.

Renal

Allergic interstitial nephritis resulting in nonoliguric renal failure has been described in a number of case reports. Several of the cases have included symptoms of rash, fever, and arthralgia and have been accompanied by eosinophilia and eosinophiluria. The cases of allergic interstitial nephritis have often responded to short courses of corticosteroid therapy.

Renal side effects have included increases in serum creatinine, BUN, and uric acid. Renal failure, interstitial nephritis, nephritis, and renal calculi have been reported in less than 1% of patients. Decreased BUN and decreased uric acid have also been reported.

Hepatic

Hepatic side effects have included cholestatic jaundice and hepatitis in less than 1% of patients. Hepatic necrosis, hepatic failure (including fatal cases), jaundice, and increased ALT, AST, alkaline phosphatase, LDH, serum bilirubin, and serum GGT have also been reported.

Musculoskeletal

Arthropathy is primarily a concern in pediatric patients. However, at least one case was described in an adult cystic fibrosis patient receiving ciprofloxacin. Although cystic fibrosis arthropathy (CFA) and hypertrophic pulmonary osteoarthropathy (HPOA) typically occur in 7% to 8% of the cystic fibrosis adult and adolescent population, the arthropathy exhibited in this patient did not resemble either. Several elements in its presentation strongly support the diagnosis of ciprofloxacin-induced arthropathy, such as: a consistent time of onset with other reported cases of suspected quinolone-induced arthropathy (usually 3 weeks after initiating therapy); a lack of history of arthralgia in the patient; reoccurrence upon rechallenge; and resolution of symptoms upon discontinuation of therapy (usually 2 weeks after termination of therapy).

Tendinitis with subsequent tendon rupture has been documented in a number of case reports. One patient with chronic renal failure developed bilateral Achilles tendon rupture after four days of ciprofloxacin therapy. Although renal transplant patients and those with end-stage renal disease tend to have an increased risk of Achilles tendinitis and rupture over the general population, quinolone use has been shown to further increase that risk (12% in quinolone-treated patients vs. 7% in nonquinolone-treated patients).

Twenty-five cases of Achilles tendon rupture have been reported to the FDA as of October 1994. Some ruptures have also occurred in the hand or shoulder. Other risk factors identified include age and corticosteroid use.

Musculoskeletal side effects have included jaw, neck, and back pain, neck and chest pain, arthralgia, joint stiffness, joint swelling, muscle spasms, night cramps, achiness, muscle weakness, and gout flare-up in less than 1% of patients. Knee inflammation, hypertonia, myoclonus, myasthenia, tendinitis, tendon rupture, myalgia, and suspected cases of reversible arthropathy have also been reported.

Cardiovascular

Cardiovascular side effects have included angina pectoris, arrhythmia, atrial flutter, cardiac murmur, cardiopulmonary arrest, cardiovascular collapse, cerebral thrombosis, hypertension, hypotension, migraine, myocardial infarction, palpitations, phlebitis, tachycardia, vasodilation, ventricular bigeminy, abdominal aortic bruit, and ventricular ectopy in less than 1% of patients. QT prolongation, torsades de pointes, ventricular arrhythmia, and postural hypotension have also been reported.

Hematologic

Hematologic side effects have included lymphadenopathy and petechiae in less than 1% of patients. Eosinophilia (0.6%), leukopenia (0.4%), decreased platelets (0.1%), increased platelets (0.1%), pancytopenia (0.1%), agranulocytosis, anemia, bleeding diathesis, bone marrow depression, decreased hemoglobin, decreased leukocytes, increased atypical lymphocyte count, immature white blood cells, increased monocytes, leukocytosis, prolongation of prothrombin time, hemolytic anemia, decreased hematocrit, thrombocytopenia, elevated sedimentation rate, decreased prothrombin time, neutropenia, life-threatening or fatal pancytopenia, and methemoglobinemia have also been reported.

Metabolic

Metabolic side effects have included acidosis; increases in serum calcium, serum amylase, lipase, triglycerides, cholesterol, blood glucose, serum creatine phosphokinase, and serum potassium; and decreases in serum albumin, serum potassium, total serum protein, and blood glucose. Quinolone class antibiotics have been associated with symptomatic hypoglycemia.

Respiratory

Respiratory side effects have included bronchospasm, dyspnea, epistaxis, hemoptysis, hiccough, laryngeal or pulmonary edema, pleural effusion, pulmonary embolism, respiratory arrest, and respiratory distress in less than 1% of patients. Wheeze, cough, upper respiratory tract infection, pharyngitis, and nasopharyngitis have also been reported.

Ocular

Ocular side effects have included decreased visual acuity, blurred vision, visual disturbances (flashing lights, overbrightness of lights, change in color perception), chromatopsia, diplopia, nystagmus, and eye pain. Quinolone class antibiotics have been associated with cataracts and multiple punctate lenticular opacities.

Psychiatric

Psychiatric side effects have included anxiety, catatonia, confusion, delirium, depersonalization, depression, hallucinations, manic reaction, nightmares, paranoia, phobia, and toxic psychosis in less than 1% of patients.

Genitourinary

Crystalluria has been reported in patients with alkaline urine and does not necessarily lead to nephrotoxicity. At physiological urinary pH, the risk of crystalluria is considered minor.

Genitourinary side effects have included albuminuria, breast pain, candiduria, cylindruria, crystalluria, frequent urination, gynecomastia, hematuria, hemorrhagic cystitis, polyuria, urethral bleeding, urinary retention, urinary tract infection, fungal vaginosis, bacterial vaginitis, dysuria, abnormal urine odor, female genital pruritus, and vaginitis in less than 1% of patients. Vaginal candidiasis, vaginal infection, urinary frequency, and micturition urgency have also been reported. Vaginal pruritus has been reported during postmarketing experience.

Other

Other side effects have included pain, foot or extremity pain, fatigue, suprapubic pain, rigors, tenderness, fungal infection, and increased body temperature. Oral ciprofloxacin has been associated with a case of Jarisch-Herxheimer reaction, characterized by hypotension, tachycardia, and disseminated intravascular coagulation, in a 14-year-old female with tickborne relapsing fever.

Disclaimer: Every effort has been made to ensure that the information provided is accurate, up-to-date, and complete, but no guarantee is made to that effect. In addition, the drug information contained herein may be time sensitive and should not be utilized as a reference resource beyond the date hereof. This information does not endorse drugs, diagnose patients, or recommend therapy. This drug information is a reference resource designed as supplement to, and not a substitute for, the expertise, skill , knowledge, and judgement of healthcare practitioners in patient care. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug of drug combination is safe, effective, or appropriate for any given patient. Drugs.com does not assume any responsibility for any aspect of healthcare administered with the aid of information provided. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse, or pharmacist.