Ciprofloxacin Hydrochloride description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Ciprofloxacin Hydrochloride

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

BOXED WARNING

WARNINGS

CIPROFLOXACIN HYDROCHLORIDE DESCRIPTION



DESCRIPTION

Ciprofloxacin Hydrochloride



Ciprofloxacin Hydrochloride




CLINICAL PHARMACOLOGY

Absorption:


Dose (mg)Maximum Serum Concentration (Area Under Curve (AUC) (hr/mL)







Distribution:


Metabolism:
CONTRAINDICATIONSWARNINGSPRECAUTIONS: Drug Interactions

Excretion:


Drug-drug Interactions:
PRECAUTIONS

CONTRAINDICATIONS
WARNINGS:PRECAUTIONS

Special Populations:
PRECAUTIONS: Geriatric Use
DOSAGE AND ADMINISTRATION




MICROBIOLOGY



INDICATIONS AND USAGE


INDICATIONS AND USAGEINHALATIONAL ANTHRAXADDITIONAL INFORMATION






Susceptibility Tests

Dilution Techniques:











**



Diffusion Techniques:





















INDICATIONS & USAGE

DOSAGE AND ADMINISTRATION

Adult Patients:














Pediatric patients (1 to 17 years of age):

WARNINGS,PRECAUTIONS, Pediatric Use,ADVERSE REACTIONSCLINICAL STUDIESANIMAL PHARMACOLOGY

Adult and Pediatric Patients:

INHALATIONAL ANTHRAXADDITIONAL INFORMATION



CIPROFLOXACIN HYDROCHLORIDE CONTRAINDICATIONS


PRECAUTIONS: Drug Interactions

WARNINGS

Tendinopathy and Tendon Rupture


Pregnant Women:
PRECAUTIONS: Pregnancy,Nursing Mothers

Pediatrics:
INDICATIONS AND USAGEADVERSE REACTIONS
ANIMAL PHARMACOLOGY

Cytochrome P450 (CYP450):


Central Nervous System Disorders:
PRECAUTIONS: GeneralInformation for PatientsDrug InteractionsADVERSE REACTIONS.

Theophylline:


Hypersensitivity Reactions:


  • ●vasculitis; arthralgia; myalgia; serum sickness;
  • ●allergic pneumonitis;
  • ●interstitial nephritis; acute renal insufficiency or failure;
  • ●hepatitis; jaundice; acute hepatic necrosis or failure;
  • ●anemia, including hemolytic and aplastic; thrombocytopenia, including thrombotic thrombocytopenic purpura; leukopenia; agranulocytosis; pancytopenia; and/or other hematologic abnormalities.
  • ●The drug should be discontinued immediately at the first appearance of a skin rash, jaundice, or any other sign of hypersensitivity and supportive measures instituted (SeePRECAUTIONS: Information for PatientsandADVERSE REACTIONS).

Pseudomembranous Colitis:




Peripheral neuropathy:


Syphilis:


PRECAUTIONS

General:
ANIMAL PHARMACOLOGY

Central Nervous System:
WARNINGSInformation for Patients,Drug Interactions

Renal Impairment:
DOSAGE AND ADMINISTRATION

Photosensitivity/Phototoxicity:




INFORMATION FOR PATIENTS


  • ●that antibacterial drugs including ciprofloxacin hydrochloride tablets should only be used to treat bacterial infections. They do not treat viral infections (e.g., the common cold). When ciprofloxacin hydrochloride tablets are prescribed to treat a bacterial infection, patients should be told that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed. Skipping doses or not completing the full course of therapy may (1) decrease the effectiveness of the immediate treatment and (2) increase the likelihood that bacteria will develop resistance and will not be treatable by ciprofloxacin hydrochloride tablets or other antibacterial drugs in the future.
  • ●that ciprofloxacin may be taken with or without meals and to drink fluids liberally. As with other quinolones, concurrent administration of ciprofloxacin with magnesium/aluminum antacids, or sucralfate, Videx
  • ●that ciprofloxacin may be associated with hypersensitivity reactions, even following a single dose, and to discontinue the drug at the first sign of a skin rash or other allergic reaction.
  • ●that photosensitivity/phototoxicity has been reported in patients receiving quinolones. Patients should minimize or avoid exposure to natural or artificial sunlight (tanning beds or UVA/B treatment) while taking quinolones. If patients need to be outdoors while using quinolones, they should wear loose-fitting clothes that protect skin from sun exposure and discuss other sun protection measures with their physician. If a sunburn-like reaction or skin eruption occurs, patients should contact their physician.
  • ●that peripheral neuropathies have been associated with ciprofloxacin use. If symptoms of peripheral neuropathy including pain, burning, tingling, numbness and/or weakness develop, they should discontinue treatment and contact their physicians.
  • ●that ciprofloxacin may cause dizziness and lightheadedness; therefore, patients should know how they react to this drug before they operate an automobile or machinery or engage in activities requiring mental alertness or coordination.
  • ●that ciprofloxacin increases the effects of tizanidine (ZanaflexPatients should not use ciprofloxacin if they are already taking tizanidine.
  • ●that ciprofloxacin may increase the effects of theophylline and caffeine. There is a possibility of caffeine accumulation when products containing caffeine are consumed while taking quinolones.
  • ●that convulsions have been reported in patients receiving quinolones, including ciprofloxacin, and to notify their physician before taking this drug if there is a history of this condition.
  • ●that ciprofloxacin has been associated with an increased rate of adverse events involving joints and surrounding tissue structures (like tendons) in pediatric patients (less than 18 years of age). Parents should inform their child's physician if the child has a history of joint-related problems before taking this drug. Parents of pediatric patients should also notify their child's physician of any joint-related problems that occur during or following ciprofloxacin therapy. (SeeWARNINGS,PRECAUTIONS, Pediatric UseandADVERSE REACTIONS.)
  • ●that diarrhea is a common problem caused by antibiotics which usually ends when the antibiotic is discontinued. Sometimes after starting treatment with antibiotics, patients can develop watery and bloody stools (with or without stomach cramps and fever) even as late as two or more months after having taken the last dose of the antibiotic. If this occurs, patients should contact their physician as soon as possible.

DRUG INTERACTIONS


WARNINGS

DOSAGE AND ADMINISTRATION










CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY



















PREGNANCY

Teratogenic Effects. Pregnancy Category C:



WARNINGS
WARNINGS

NURSING MOTHERS



PEDIATRIC USE

ANIMAL PHARMACOLOGY

DOSAGE AND ADMINISTRATIONINHALATIONAL ANTHRAXADDITIONAL INFORMATION

ADVERSE REACTIONSCLINICAL STUDIES




GERIATRIC USE

Boxed WarningWARNINGS
CLINICAL PHARMACOLOGYDOSAGE AND ADMINISTRATION


CIPROFLOXACIN HYDROCHLORIDE ADVERSE REACTIONS




















Adverse Reactions in Pediatric Patients:





CiprofloxacinComparator





Post-Marketing Adverse Event Reports:

PRECAUTIONS
INHALATIONAL ANTHRAX - ADDITIONAL INFORMATION







OVERDOSAGE




DOSAGE & ADMINISTRATION

Dosage Guidelines table



InfectionSeverityDoseFrequencyUsual Durations


INHALATIONAL ANTHRAXADDITIONAL INFORMATION

Conversion of I.V. to Oral Dosing in Adults:
CLINICAL PHARMACOLOGY

Equivalent AUC Dosing Regimens
Ciprofloxacin Oral DosageEquivalent Ciprofloxacin I.V. Dosage
Adults with Impaired Renal Function:


RECOMMENDED STARTING AND MAINTENANCE DOSES FOR PATIENTS WITH IMPAIRED RENAL FUNCTION
Creatinine Clearance (mL/min)Dose




DOSAGE AND ADMINISTRATION - PEDIATRICS
Dosage Guidelines tableADVERSE REACTIONSCLINICAL STUDIES




INHALATIONAL ANTHRAXADDITIONAL INFORMATION



HOW SUPPLIED





ANIMAL PHARMACOLOGY & OR TOXICOLOGY

WARNINGS




CLINICAL STUDIES

Complicated Urinary Tract Infection and PyelonephritisEfficacy in Pediatric Patients:






CiprofloxacinComparator

INHALATIONAL ANTHRAX IN ADULTS AND PEDIATRICSADDITIONAL INFORMATION
DOSAGE AND ADMINISTRATIONPRECAUTIONS, Pediatric Use





REFERENCES













SPL MEDGUIDE




  • ●Tendons are tough cords of tissue that connect muscles to bones.
  • ●Pain, swelling, tears and inflammation of tendons including the back of the ankle (Achilles), shoulder, hand, or other tendon sites can happen in people of all ages who take fluoroquinolone antibiotics, including ciprofloxacin hydrochloride tablets. The risk of getting tendon problems is higher if you:
  • ●are over 60 years of age
  • ●are taking steroids (corticosteroids)
  • ●have had a kidney, heart or lung transplant.
  • ●Swelling of the tendon (tendinitis) and tendon rupture (breakage) have also happened in patients who take fluoroquinolones who do not have the above risk factors.
  • ●Other reasons for tendon ruptures can include:
  • ●physical activity or exercise
  • ●kidney failure
  • ●tendon problems in the past, such as in people with rheumatoid arthritis (RA)
  • ●Call your healthcare provider right away at the first sign of tendon pain, swelling or inflammation. Stop taking ciprofloxacin hydrochloride tablets until tendinitis or tendon rupture has been ruled out by your healthcare provider. Avoid exercise and using the affected area. The most common area of pain and swelling is the Achilles tendon at the back of your ankle. This can also happen with other tendons. Talk to your healthcare provider about the risk of tendon rupture with continued use of ciprofloxacin hydrochloride tablets. You may need a different antibiotic that is not a fluoroquinolone to treat your infection.
  • ●Tendon rupture can happen while you are taking or after you have finished taking ciprofloxacin hydrochloride tablets. Tendon ruptures have happened up to several months after patients have finished taking their fluoroquinolone.
  • ●Get medical help right away if you get any of the following signs or symptoms of a tendon rupture:
  • ●hear or feel a snap or pop in a tendon area
  • ●bruising right after an injury in a tendon area
  • ●unable to move the affected area or bear weight
  • ●See the sectionWhat are the possible side effects of ciprofloxacin hydrochloride tablets?for more information about side effects.
  • ●What are ciprofloxacin hydrochloride tablets?







  • ●also take a medicine called tizanidine (Zanaflex). Serious side effects from tizanidine are likely to happen.
  • ●What should I tell my healthcare provider before taking ciprofloxacin hydrochloride tablets?



  • ●have central nervous system problems (such as epilepsy)
  • ●have nerve problems
  • ●have or anyone in your family has an irregular heartbeat, especially a condition calledQT prolongation
  • ●have a history of seizures
  • ●have kidney problems. You may need a lower dose of ciprofloxacin hydrochloride tablets if your kidneys do not work well.
  • ●have rheumatoid arthritis (RA) or other history of joint problems
  • ●have trouble swallowing pills
  • ●are pregnant or planning to become pregnant. It is not known if ciprofloxacin hydrochloride tablets will harm your unborn child.
  • ●are breast-feeding or planning to breast-feed. Ciprofloxacin hydrochloride tablets passes into breast milk. You and your healthcare provider should decide whether you will take ciprofloxacin hydrochloride tablets or breast-feed.
  • ●Tell your healthcare provider about all the medicines you take, including prescription and non-prescription medicines, vitamins and herbal and dietary supplements. Ciprofloxacin hydrochloride tablets and other medicines can affect each other causing side effects. Especially tell your healthcare provider if you take:

  • ●a blood thinner (warfarin, CoumadinJantoven
  • ●tizanidine (ZanaflexYou should not take ciprofloxacin hydrochloride tablets if you are already taking tizanidine. SeeWho should not take ciprofloxacin hydrochloride tablets?
  • ●theophylline (Theo-24ElixophyllinTheochronUniphylTheolair
  • ●glyburide (MicronaseGlynaseDiabetaGlucovanceSeeWhat are the possible side effects of ciprofloxacin hydrochloride tablets?
  • ●phenytoin (Fosphenytoin SodiumCerebyxDilantin-125DilantinExtended Phenytoin SodiumPrompt Penytoin SodiumPhenytek
  • ●products that contain caffeine
  • ●a medicine to control your heart rate or rhythm (antiarrhythmics) SeeWhat are the possible side effects of ciprofloxacin hydrochloride tablets?
  • ●an anti-psychotic medicine
  • ●a tricyclic antidepressant
  • ●a water pill (diuretic)
  • ●a steroid medicine. Corticosteroids taken by mouth or by injection may increase the chance of tendon injury. SeeWhat is the most important information I should know about ciprofloxacin hydrochloride tablets?
  • ●methotrexate (Trexall
  • ●Probenecid (ProbalanCol-probenecid
  • ●Metoclopromide (ReglanReglan ODT
  • ●Certain medicines may keep ciprofloxacin hydrochloride tablets from working correctly. Take ciprofloxacin hydrochloride tablets either 2 hours before or 6 hours after taking these products:
  • ●an antacid, multivitamin, or other product that has magnesium, calcium, aluminum, iron, or zinc
  • ●sucralfate (Carafate
  • ●didanosine (VidexVidexEC).
  • ●Ask your healthcare provider if you are not sure if any of your medicines are listed above.



  • ●Take ciprofloxacin hydrochloride tablets in the morning and evening at about the same time each day. Swallow the tablet whole. Do not split, crush or chew the tablet. Tell your healthcare provider if you can not swallow the tablet whole.
  • ●Ciprofloxacin hydrochloride tablets can be taken with or without food.
  • ●Ciprofloxacin hydrochloride tablets should not be taken with dairy products (like milk or yogurt) or calcium-fortified juices alone, but may be taken with a meal that contains these products.
  • ●Drink plenty of fluids while taking ciprofloxacin hydrochloride tablets.
  • ●Do not skip any doses, or stop taking ciprofloxacin hydrochloride tablets even if you begin to feel better, until you finish your prescribed treatment, unless:
  • ●you have tendon effects (seeWhat is the most important information I should know about ciprofloxacin hydrochloride tablets?),
  • ●you have a serious allergic reaction (seeWhat are the possible side effects of ciprofloxacin hydrochloride tablets?), or your healthcare provider tells you to stop.
  • ●This will help make sure that all of the bacteria are killed and lower the chance that the bacteria will become resistant to ciprofloxacin hydrochloride tablets. If this happens, ciprofloxacin hydrochloride tablets and other antibiotic medicines may not work in the future.
  • ●If you miss a dose of ciprofloxacin hydrochloride tablets, take it as soon as you remember. Do not take two doses at the same time, and do not take more than two doses in one day.
  • ●If you take too much, call your healthcare provider or get medical help immediately.
  • ●If you have been prescribed ciprofloxacin hydrochloride tablets after being exposed to anthrax:

  • ●Take ciprofloxacin hydrochloride tablets exactly as prescribed by your healthcare provider. Do not stop taking ciprofloxacin hydrochloride tablets without talking with your healthcare provider. If you stop taking ciprofloxacin hydrochloride tablets too soon, it may not keep you from getting the anthrax disease.
  • ●Side effects may happen while you are taking ciprofloxacin hydrochloride tablets. When taking your ciprofloxacin hydrochloride tablets to prevent anthrax infection, you and your healthcare provider should talk about whether the risks of stopping ciprofloxacin hydrochloride tablets too soon are more important than the risks of side effects with ciprofloxacin hydrochloride tablets.
  • ●If you are pregnant, or plan to become pregnant while taking ciprofloxacin hydrochloride tablets, you and your healthcare provider should decide whether the benefits of taking ciprofloxacin hydrochloride tablets for anthrax are more important than the risks.
  • ●What should I avoid while taking ciprofloxacin hydrochloride tablets?

  • ●Avoid sunlamps, tanning beds, and try to limit your time in the sun. Ciprofloxacin hydrochloride tablets can make your skin sensitive to the sun (photosensitivity) and the light from sunlamps and tanning beds. You could get severe sunburn, blisters or swelling of your skin. If you get any of these symptoms while taking ciprofloxacin hydrochloride tablets, call your healthcare provider right away. You should use a sunscreen and wear a hat and clothes that cover your skin if you have to be in sunlight.
  • ●What are the possible side effects of ciprofloxacin hydrochloride tablets?


  • ●Seizures have been reported in people who take fluoroquinolone antibiotics including ciprofloxacin hydrochloride tablets. Tell your healthcare provider if you have a history of seizures. Ask your healthcare provider whether taking ciprofloxacin hydrochloride tablets will change your risk of having a seizure. Central Nervous System (CNS) side effects may happen as soon as after taking the first dose of ciprofloxacin hydrochloride tablets. Talk to your healthcare provider right away if you get any of these side effects, or other changes in mood or behavior:
  • ●feel dizzy
  • ●seizures
  • ●hear voices, see things, or sense things that are not there (hallucinations)
  • ●feel restless
  • ●tremors
  • ●feel anxious or nervous
  • ●confusion
  • ●depression
  • ●trouble sleeping
  • ●nightmares
  • ●feel more suspicious (paranoia)
  • ●suicidal thoughts or acts
  • ●Serious allergic reactions
  • ●Allergic reactions can happen in people taking fluoroquinolones, including ciprofloxacin hydrochloride tablets, even after only one dose. Stop taking ciprofloxacin hydrochloride tablets and get emergency medical help right away if you get any of the following symptoms of a severe allergic reaction:
  • ●hives
  • ●trouble breathing or swallowing
  • ●swelling of the lips, tongue, face
  • ●throat tightness, hoarseness
  • ●rapid heartbeat
  • ●faint
  • ●yellowing of the skin or eyes.
  • ●Stop taking ciprofloxacin hydrochloride tablets and tell your healthcare provider right away if you get yellowing of your skin or white part of your eyes, or if you have dark urine. These can be signs of a serious reaction to ciprofloxacin hydrochloride tablets (a liver problem).
  • ●Skin rash
  • ●Skin rash may happen in people taking ciprofloxacin hydrochloride tablets, even after only one dose. Stop taking ciprofloxacin hydrochloride tablets at the first sign of a skin rash and call your healthcare provider. Skin rash may be a sign of a more serious reaction to ciprofloxacin hydrochloride tablets.
  • ●Serious heart rhythm changes (QT prolongation and torsade de pointes)
  • ●Tell your healthcare provider right away if you have a change in your heart beat (a fast or irregular heartbeat), or if you faint. Ciprofloxacin hydrochloride tablets may cause a rare heart problem known as prolongation of the QT interval. This condition can cause an abnormal heartbeat and can be very dangerous. The chances of this event are higher in people:
  • ●who are elderly
  • ●with a family history of prolonged QT interval
  • ●with low blood potassium (hypokalemia)
  • ●who take certain medicines to control heart rhythm (antiarrhythmics)
  • ●Intestine infection (Pseudomembranous colitis)
  • ●Pseudomembranous colitis can happen with most antibiotics, including ciprofloxacin hydrochloride tablets. Call your healthcare provider right away if you get watery diarrhea, diarrhea that does not go away, or bloody stools. You may have stomach cramps and a fever. Pseudomembranous colitis can happen 2 or more months after you have finished your antibiotic.
  • ●Changes in sensation and possible nerve damage (Peripheral Neuropathy)
  • ●Damage to the nerves in arms, hands, legs, or feet can happen in people who take fluoroquinolones, including ciprofloxacin hydrochloride tablets. Talk with your healthcare provider right away if you get any of the following symptoms of peripheral neuropathy in your arms, hands, legs, or feet:
  • ●pain
  • ●burning
  • ●tingling
  • ●numbness
  • ●weakness
  • ●Ciprofloxacin hydrochloride tablets may need to be stopped to prevent permanent nerve damage.

  • ●People who take ciprofloxacin hydrochloride tablets and other fluoroquinolone medicines with the oral anti-diabetes medicine glyburide (Micronase, Glynase, Diabeta, Glucovance) can get low blood sugar (hypoglycemia) which can sometimes be severe. Tell your healthcare provider if you get low blood sugar with ciprofloxacin hydrochloride tablets. Your antibiotic medicine may need to be changed.
  • ●Sensitivity to sunlight (photosensitivity)
  • ●SeeWhat should I avoid while taking ciprofloxacin hydrochloride tablets?
  • ●Joint Problems
  • ●Increased chance of problems with joints and tissues around joints in children under 18 years old. Tell your child's healthcare provider if your child has any joint problems during or after treatment with ciprofloxacin hydrochloride tablets.
  • ●The most common side effects of ciprofloxacin hydrochloride tablets include:

  • ●headache
  • ●diarrhea
  • ●vomiting
  • ●vaginal yeast infection
  • ●changes in liver function tests pain or discomfort in the abdomen
  • ●These are not all the possible side effects of ciprofloxacin hydrochloride tablets. Tell your healthcare provider about any side effect that bothers you, or that does not go away.



  • ●Store ciprofloxacin hydrochloride tablets at 20(68(59
  • ●Keep ciprofloxacin hydrochloride tablets and all medicines out of the reach of children.





  • ●Active ingredient: ciprofloxacin
  • ●Inactive ingredients: cornstarch, microcrystalline cellulose, silicon dioxide, crospovidone, magnesium stearate, polyvinyl alcohol, talc, titanium dioxide, polyethylene glycol and purified water
  • ●This Medication Guide has been approved by the U.S. Food and Drug Administration.






PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Ciprofloxacin Hydrochloride



Ciprofloxacin Hydrochloride






Ciprofloxacin Hydrochloride

Ciprofloxacin Hydrochloride TABLET, FILM COATED

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-194(NDC:16252-515)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CIPROFLOXACIN HYDROCHLORIDE CIPROFLOXACIN 500 mg

Inactive Ingredients

Ingredient Name Strength
STARCH, CORN
cellulose, microcrystalline
SILICON DIOXIDE
CROSPOVIDONE
MAGNESIUM STEARATE
POLYVINYL ALCOHOL
talc
titanium dioxide
polyethylene glycol

Product Characteristics

Color Size Imprint Code Shape
white 18 mm CR;500 CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-194-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076794 2011-04-20


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.