Treatment of bacterial infections of the lungs, nose, ear, bones and joints, skin and soft tissue, kidney, bladder, abdomen, and genitals caused by ciprofloxacin-susceptible organisms. Infections may include urinary tract infection, prostatitis, lower respiratory tract infection, otitis media (middle ear infection), sinusitis, skin, bone and joint infections, infectious diarrhea, typhoid fever, and gonorrhea.
May be taken with or without food. May be taken w/ meals to minimise GI discomfort. Do not take w/ antacids, Fe or dairy products.
Hypersensitivity to ciprofloxacin or other quinolones. History or risk of QT prolongation; known history of myasthenia gravis. Concomitant use with tizanidine.
Vomiting, Stomach pain, Nausea, Diarrhea
Patient with known or suspected CNS disorders, risk factors predisposing to seizures, or lower seizure threshold; history or risk factors for QT interval prolongation, torsades de pointes, uncorrected hypokalaemia/hypomagnesaemia, cardiac disease (e.g. heart failure, MI, bradycardia); positive family history of aneurysm disease, pre-existing aortic aneurysm or dissection and its risk factors (e.g. Marfan syndrome, vascular Ehlers-Danlos syndrome, hypertension, peripheral atherosclerotic vascular disease); diabetes, previous tendon disorder (e.g. rheumatoid arthritis), G6PD deficiency. Renal and hepatic impairment. Elderly, children. Pregnancy and lactation.
Store between 20-25°C.
Quinolones
Use on private or community delivery only.quinolone antibiotics
Azithromycin 500mgBacterial infection, dizziness, nausea, diarrhea, thrombocytopenia, vasodilatation, thrombosis, UGitonosis, respiratory depression, hypotension, renal impairment, hepatic impairment, bone marrow dysfunction, depression, fatigue, fever, abdominal pain, abdominal swelling, muscle pain, dizziness, lethargic, patient changes, mental and neurological changes.
idespread dermatological skin rash, acne, allergic disorders, skin rashes, eczema, itching, erythema, rash, urticaria, and rashes. Bone and joint infections, acne, dermatitis, dermatitis, dermatitis herder, dermatitis, hives, generalized dermatitis, generalized hives, myalgia, pain, rash, swelling, rash, sweating, and sweating. Post-herpetic neuralgia, postoperative dermatitis, nervousness, tremor, seizures, and post-extensive body weight loss. Sulfamethoxazole and sulfamethoxazole and their sulfa drugs, and trimethoprim and sulfa drug.The safety and efficacy of using ciprofloxacin during pregnancy has not been established. Consider using of ciprofloxacin during pregnancy if necessary.
It is recommended to use ciprofloxacin with milk if possible for a limited time. Consider the time it takes for breast-feeding, especially if it is aintestines.
Dairy and Fecommunication Concerns - Ciprofloxacin May Cause Cerebral Yourelin Defining the 'Transmission' of Bacterial Infections. The Cerebral Yourelin Defining the 'Transmission' of Bacterial Infections. The Cerebralyourelin Defining the 'Transmission' of Bacterial Infections. Ciprofloxacin May Cause Cerebral Yourelin Defining the 'Transmission' of Bacterial Infections.Treatment of bacterial infections of the lungs, nose, ear, bones and joints, skin and soft tissue, kidney, bladder, abdomen, and genitals caused by ciprofloxacin-susceptible organisms. Infections may include urinary tract infection, prostatitis, lower respiratory tract infection, otitis media (middle ear infection), sinusitis, skin, bone and joint infections, infectious diarrhea, typhoid fever, and gonorrhea.
May be taken with or without food. May be taken w/ meals to minimise GI discomfort. Do not take w/ antacids, Fe or dairy products.
Hypersensitivity to ciprofloxacin or other quinolones. History or risk of QT prolongation; known history of myasthenia gravis. Concomitant use with tizanidine.
Vomiting, Stomach pain, Nausea, Diarrhea
Patient with known or suspected CNS disorders, risk factors predisposing to seizures, or lower seizure threshold; history or risk factors for QT interval prolongation, torsades de pointes, uncorrected hypokalaemia/hypomagnesaemia, cardiac disease (e.g. heart failure, MI, bradycardia); positive family history of aneurysm disease, pre-existing aortic aneurysm or dissection and its risk factors (e.g. Marfan syndrome, vascular Ehlers-Danlos syndrome, hypertension, peripheral atherosclerotic vascular disease); diabetes, previous tendon disorder (e.g. rheumatoid arthritis), G6PD deficiency. Renal and hepatic impairment. Elderly, children. Pregnancy and lactation.
Store between 20-25°C.
Quinolones
MedsGo Class UnknownNuva Tablet, 100mgBe aware of:Active ingredient:ciprofloxacin-susceptible organisms.Inactive ingredients:annabinoids, colloidal silicon dioxide, glycerin, water retention, hypromellose, hydroxypropylcellulose, iron oxide, iron oxide 600, iron oxide red, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, sodium starch glycolate, talc, titanium dioxide, triethyl citrate
Alcon Tablet, 100mgCiprofloxacin is a broad-spectrum antibiotic belonging to the fluoroquinolone class. It is prescribed for the treatment of various bacterial infections, including urinary tract infections (UTIs), respiratory tract infections, skin and soft tissue infections, sexually transmitted diseases, and certain types of blood dyscrasias.
In addition to the above-mentioned indications, Ciprofloxacin is also used for the prevention of anthrax in the lungs, in the skin, and in certain other infections, including pneumonia and bronchitis.
Cipla, India’s largest pharmaceutical manufacturer, is the leading manufacturer of Ciprofloxacin tablets and other pharmaceutical products in the Indian market. The company also manufactures and distributes the generic version of Ciprofloxacin.
Ciprofloxacin tablets are used to treat various bacterial infections caused by susceptible bacteria.
The tablets are manufactured by the company in India and supplied by the company as a sterile, effervescent solution.
The tablets should be taken orally with a full glass of water, preferably within 15-30 minutes after reconstituting. The medication can be taken with or without food.
Ciprofloxacin tablets should be used only when prescribed by a healthcare professional.
The tablets should be swallowed whole with a glass of water.
The dosage of Ciprofloxacin tablets is the same as that of other drugs used for treating bacterial infections. The recommended dose is one 500 mg tablet taken orally three times a day, with or without food.
Ciprofloxacin tablets should be taken with a full glass of water, preferably within 15-30 minutes after reconstituting.
The dosage of Ciprofloxacin tablets may vary depending on the type of bacteria causing the infection. The usual dosage is one 500 mg tablet taken orally three times a day, with or without food.
The common side effects of Ciprofloxacin tablets are nausea, diarrhea, headache, and dizziness.
Product
Ciprofloxacin (Cipro) is a quinolone antibacterial agent used to treat various infections caused by bacteria in different parts of the body including skin, soft tissue, bone, joints and urinary tract. It is antibacterial in nature, acts as a prodrug (which inhibits a bacteria’s ability to grow and multiply) and is effective against a wide range of Gram-positive and Gram-negative bacteria.
Cipro contains two medicines, Ciprofloxacin and Cipro-Trimethoprim, and it is used to treat bacterial infections of the skin, joints and urinary tract caused by gram-negative and gram-positive bacteria. Ciprofloxacin is used to treat infections of the skin caused by Mycoplasma. Cipro-Trimethoprim contains trimethoprim as a preservative. It is used to treat infections caused by Escherichia coli and Klebsiella spp. Ciprofloxacin is used to treat skin infections caused by Neisseria gonorrhoeae. It is also used to treat urinary tract infections due to the bactericidal action of Cipro.
Ciprofloxacin
Ciprofloxacin is a fluoroquinolone antibiotic. It works by killing bacteria and preventing their growth. It is commonly used for the treatment of infections of the skin, joints and urinary tract caused by Mycoplasma. It is used to treat skin infections due to the bactericidal action of Cipro.
Cipro-Trimethoprim
Cipro-Trimethoprim is a generic medication containing the generic fluoroquinolone antibiotic ciprofloxacin. Cipro-Trimethoprim is used to treat infections of the skin, joints and urinary tract caused by Mycoplasma. Cipro-Trimethoprim is also used to treat skin and soft tissue infections in bone and joints caused by Neisseria gonorrhoeae. Cipro-Trimethoprim is also used to treat urinary tract infections due to the bactericidal action of ciprofloxacin.
It is used to treat skin infections due to the bactericidal action of ciprofloxacin. Ciprofloxacin is also used to treat urinary tract infections due to the bactericidal action of trimethoprim.
Show moreThe drug of choice for infections in the skin, joints and urinary tract caused by Mycoplasma is trimethoprim.
Ciprofloxacin (CiproHCL), a white to off-white powder, is an antibiotic belonging to the fluoroquinolone family. Ciprofloxacin monohydrate is used to treat a wide range of bacterial infections, including:
Mechanism of Action
Ciprofloxacin (CiproHCL) is a fluoroquinolone which belongs to the quinolone class of antibiotics. It inhibits bacterial DNA gyrase, topoisomerase IV, and topoisomerase IV enzymes, which in turn kills the bacteria and prevents them from multiplying.
Pharmacological Properties
Ciprofloxacin monohydrate has a broad spectrum of activity against a wide range of bacteria, including:
Pharmacokinetics
Ciprofloxacin monohydrate is well absorbed from the gastrointestinal tract (1):
After oral administration it is rapidly and extensively distributed to the entire body. The average peak concentration is reached in about 2 hours and the area under the blood-clotting curve (AUC) is about 3 times higher than that in normal volunteers. The half-life is about 4 hours, which is longer than that in healthy volunteers.
Resistance to Various Antibiotics
Ciprofloxacin monohydrate is highly effective against a wide range of bacteria. The antibiotic is most effective against Pseudomonas aeruginosa, Haemophilus influenzae, Chlamydia psittaci, and Mycoplasma hominis.
Following oral administration, Ciprofloxacin monohydrate is rapidly absorbed and distributed to the entire body and peak concentrations are reached in about 1 to 2 hours. A steady state plasma level (Css) is reached in about 1 to 2 hours. The average peak concentration is about 5 to 7 times higher than in normal volunteers.
Ciprofloxacin monohydrate is highly effective against a wide range of bacteria, including:
After oral administration, Ciprofloxacin monohydrate is rapidly absorbed and distributed to the entire body and peak concentrations are reached in about 2 to 3 hours. The average peak concentration is about 2 to 3 times higher than in normal volunteers. The half-life is about 5 to 7 hours.
Ciprofloxacin monohydrate is highly metabolized by cytochrome P450 enzymes and by the liver. The half-life is about 18 hours, which is longer than that in healthy volunteers. The clearance is about 5 mL/kg/day. The plasma half-life is about 3 to 4 hours, which is longer than that in healthy volunteers. The Css is about 4 times higher than in normal volunteers.
Ciprofloxacin monohydrate is a broad spectrum antibiotic.
After oral administration it is rapidly and extensively distributed to the entire body and peak concentrations are reached in about 2 to 3 hours. The AUC is about 3 times higher than that in normal volunteers. The half-life is about 2 to 3 hours, which is longer than that in healthy volunteers.
Ciprofloxacin monohydrate is a potent broad-spectrum antibiotic. The drug is highly active against a wide range of bacteria, including:
After oral administration, Ciprofloxacin monohydrate is rapidly absorbed and distributed to the entire body and peak concentrations are reached in about 1 to 2 hours.
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