Ciprofloxacin is a fluoroquinolone antibiotic, which has a broad spectrum against bacterial and protozoal pathogens. It is used in the treatment of bacterial infections and also for the prevention of postoperative infections, dental infections, urinary tract infections, and gonorrhea. It is also used in the treatment of postoperative infections following dental surgery.
Ciprofloxacin is an antibiotic that has a broad spectrum against
Ciprofloxacin works by inhibiting bacterial protein synthesis, which is essential for bacterial growth.
Ciprofloxacin is available as a tablet, suspension, and intravenous (IV) solution for oral administration.
Ciprofloxacin is an effective antibiotic that has a broad spectrum against
The dosage of ciprofloxacin depends on the type and severity of infection, patient age, body weight, concomitant medications, and specific needs. The duration of treatment depends on the type and severity of infection.
For the treatment of urinary tract infections, the dosage should be adjusted with medical supervision. The duration of treatment should be supervised to ensure the infection is completely eradicated.
For the prevention of postoperative infections, the dosage should be adjusted with medical supervision.
Before using ciprofloxacin, it is crucial to inform your doctor if you are allergic to it, have liver or kidney problems, are pregnant, breastfeeding, or planning for pregnancy. Inform your doctor about any previous medical history, current medications, or conditions.
Like all antibiotics, ciprofloxacin may cause side effects, although not everyone experiences them. Common side effects of ciprofloxacin include nausea, vomiting, diarrhea, and abdominal pain. These side effects are usually mild and subside as the body adjusts to the medication. However, it is essential to note that these side effects are rare and may occur rarely.
Ciprofloxacin may interact with other medications, especially in combination with other antibiotics. It is essential to inform your doctor about all the medications you are taking before starting ciprofloxacin. Especially, you should inform your doctor if you are taking any nitrates or amyl nitrite.
Ciprofloxacin should be stored at room temperature, away from moisture and light. Disposal of the medicine should be done at room temperature and away from direct light.
Product informationCiprofloxacin is available in the market in concentration of 500 mg/5 mL (5 mg/mL) in a tablet, solution, and suspension, and in concentration of 10 mg/mL (10 mg/mL) in a suspension.
Product descriptionThe product has a shelf life of 11 days. The product is available in the concentration of 500 mg/5 mL and 10 mg/mL. The product is supplied in an expiry date (EXP) of 14th August 2022. The expiry date of the product is not valid if the packaging has the expiration date printed on the front of the product. The product should not be disposed of in the event that the expiry date has expired.
The product is supplied in the concentration of 500 mg/5 mL and 10 mg/mL. The product is available in the concentration of 10 mg/mL and 10 mg/mL.
Cipro has been shown to cause some side effects. Talk to your health care provider if these mild reactions do not go away within a few days.
Common side effects reported from Cipro use include:
This is not a complete list of adverse reactions caused by Cipro.Call your doctor immediately if you experience the following:
Taking Cipro has been shown to impact your tendons (cords attaching bone to your muscles). It can increase your risk of developing tendonitis or a tendon rupture, especially if you’re over 60, taking steroid medications, or have a history of tendon problems.
Cipro can interact with other medications and substances, causing potentially serious side effects or allergic reactions. Tell your doctor if you are taking muscle relaxers such as tizanidine (Zanaflex), phosphodiesterase 5 (PDE5) inhibitors such as sildenafil, anticoagulants (blood thinners), antidepressants, antipsychotics, diuretics, insulin, nonsteroidal anti-inflammatory drugs (NSAIDs) like ibuprofen or naproxen.
This is not a complete list of Cipro drug interactions, so discuss any medications you’re on, even if you don’t see them listed here. Cipro can cause low blood sugar in some patients. Be wary of low blood pressure symptoms such as blurred vision, fatigue, confusion, pale skin, and cold sweats. Watch for these adverse effects if you have diabetes, and take diabetes medication orally. These could be signs of hypoglycemia and could lead to unconsciousness.
The U. S. Food and Drug Administration (FDA) has found that, while rare, fluoroquinolone antibiotics like Cipro can increase the occurrence of severe ruptures or tears in your aorta (a large artery that begins in the heart). These ruptures can lead to dangerous aortic bleeding, a heart attack, or even death, so people at risk for cardiac problems should be cautious about taking Cipro.
Be sure to tell your doctor if you have been diagnosed with or have a history of other medical conditions, including a prolonged QT interval (a rare heart problem that may cause an irregular heartbeat, fainting, or sudden death), aneurysms, kidney disease, liver disease, heart disease, myasthenia gravis (severe muscle weakness), seizures, or diabetes. Cipro can also significantly increase theophylline levels in your blood, leading to serious illness or death. This is not a comprehensive list of medical conditions that Cipro may affect, so speak with your doctor about your medical history before taking Cipro.
Cipro can cause your skin to become sensitive to sunlight or ultraviolet light, so try to avoid unnecessary sun exposure and do your best to wear protective clothing, sunglasses, or sunscreen that is SPF 15 or higher. Call your doctor if you notice redness, swelling, or blistering from sun exposure while on Cipro.
As with all prescription medication, inform the prescribing doctor about any medical conditions you have been diagnosed with and any medications or supplements you currently take before starting treatment. Antacids can reduce the amount of Cipro that your body absorbs, so be sure to take them at least 2 hours before or 6 hours after taking antacid medications.
In addition, let your doctor know if you are breastfeeding, pregnant, or planning on becoming pregnant before starting treatment with this medication.
If a patient requests aivan (Jantoven)medication, message the patient to stop taking Cipro and to stop using it immediately.
A recent study found that fluoroquinolone antibiotics (FQ) have a higher rate of antibiotic resistance than other classes of antibiotics, which makes FQ a major concern for the health care system.
FQs are used to treat infections caused by bacteria, such as urinary tract infections (UTIs), pneumonia, bronchitis, and gonorrhea, as well as certain types of skin infections, ear infections, and pneumonia. They can be expensive and often require hospitalization. It is crucial to take antibiotics with a high-quality, high-quality product, such as FQs, so they are safe and effective for the patient and are not likely to cause harm.
FQs are generally safe and effective and are prescribed by healthcare providers. However, they are not always safe and effective. The risks associated with FQs are generally low and the risk of side effects is higher. FQs may be prescribed for long periods of time, and may interact with other medications, such as certain antibiotics and certain other antibiotics, which can increase the risk of side effects.
There are no known adverse events associated with the use of FQs, and no data is available for patients who take FQs. The most common adverse events reported by patients who take FQs include:
A report of one case of serious liver injury linked to FQs in a patient who was taking a nonprescription drug indicated that the dose could be increased or decreased to achieve the same effect.
This could increase the risk of the patient developing a serious reaction, such as an allergic reaction, in the future. Patients taking FQs should not self-medicate their symptoms to ensure they do not get severe adverse events.
Patients should discuss these side effects with their healthcare provider and monitor for them closely while taking FQs. It is crucial for patients taking FQs to be monitored closely for side effects, and to report any changes to their medical records to their primary care provider immediately. Patients should also ask their doctors about other medications, such as antibiotics, if they take FQs.
For further information about the risk of side effects, including possible drug interactions, please contact your healthcare provider for medical advice.
In conclusion, FQs are generally safe and effective and are prescribed by healthcare providers. They are less likely to cause harm and may be prescribed in the same manner as antibiotics.
CIPROFLOXACIN MICROSCOPY DOSE (10 MG/ML) INJECTION FOR IVF (3 doses for 2-8 days)Oral administration of FQs has been shown to decrease the risk of antibiotic-associated side effects in clinical trials. However, it has been unclear whether FQs are more effective than antibiotics or are more likely to cause serious adverse events.
The risk of adverse events associated with oral administration of FQs appears to be low, but the incidence of these events was not reported in clinical trials. The risks are considered relatively low with these antibiotics and may be acceptable with other oral drugs. However, the incidence of serious adverse events has been increased in clinical trials with oral administration of FQs.
AUGMENTAL INFUSION (10 MG/ML) INJECTION FOR IVF (2 doses for 3 days)FQs are generally safe and are prescribed by healthcare providers. However, they may be given to patients who have been prescribed FQs, such as patients who do not have a medical history of antibiotic-associated side effects.
AUGMENTAL INFUSION (10 MG/ML) INJECTION FOR IVF (3 doses for 1-5 days)
Product name:CIPROFLOXACIN
Company name:
DIN:02357226
Status:Marketed
Status date:2024-05-26
| Active ingredient(s) | Strength |
|---|---|
| 5 MG |
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The Product Monograph is a scientific document that describes the properties, claims, indications and conditions of use of the product and contains any other information that may be required for optimal, safe and effective use. The Product Monograph includes three sections:
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Side effects are troublesome symptoms or feelings that you may not expect that show up when you are taking a medicine. All suspected side effects should be reported, especially those that are:
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Section C.01.020.1 of the Food and Drug Regulations and section 62 of the Medical Devices Regulations, require hospitals to report to Health Canada all serious adverse drug reactions (ADRs) and medical device incidents (MDIs) within 30 days of being documented within the hospital. This regulatory requirement only applies to hospitals. |
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