Arapime
Arapime Uses, Dosage, Side Effects, Food Interaction and all others data.
Arapime Hydrochloride is a preparation of Arapime. It is a fourth generation broad-spectrum cephalosporin antibiotic. Arapime acts by inhibition of bacterial cell wall synthesis. It is highly resistant to hydrolysis by most beta-lactamases and exhibits rapid penetration into gram-negative bacterial cells.
Arapime has been shown to be active against most strains of the following microorganisms:
Gram-Positive Microorganisms:
Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes, Viridans group streptococci, Staphylococcus epidermidis, Staphylococcus saprophyticus, Staphylococcus hominis, Streptococcus agalactiae.
Gram-Negative Microorganisms:
Enterobacter, Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Pseudomonas aeruginosa, Acinetobacter calcoaceticus, Citrobacter diversus, Citrobacter freundii, Enterobacter spp., Haemophilus influenzae (including beta-lactamase producing strains), Haemophilus parainfluenzae, Hafnia alvei, Klebsiella oxytoca, Moraxella catarrhalis (including beta-lactamase producing strains), Morganella morganii, Proteus vulgaris, Providencia rettgeri, Providencia stuartii, Serratia marcescens, Neisseria meningitidis.
Anaerobes:
Trade Name | Arapime |
Availability | Prescription only |
Generic | Cefepime |
Cefepime Other Names | Cefepima, Cefepime, Cefepimum |
Related Drugs | amoxicillin, doxycycline, ciprofloxacin, cephalexin, metronidazole, azithromycin, clindamycin, ceftriaxone, levofloxacin, Augmentin |
Weight | 1g, 500mg |
Type | Injection |
Formula | C19H24N6O5S2 |
Weight | Average: 480.561 Monoisotopic: 480.124959288 |
Protein binding | The serum protein binding of cefepime is approximately 20% and is independent of its concentration in serum. |
Groups | Approved, Investigational |
Therapeutic Class | Fourth generation Cephalosporins |
Manufacturer | Ar Pharmaceuticals |
Available Country | Pakistan |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
Arapime Hydrochloride is used for the treatment of the following infections:
• Pneumonia (moderate to severe)
• Uncomplicated and Complicated Urinary Tract Infections (including pyelonephritis)
• Uncomplicated Skin and Skin Structure Infections
• Complicated Intra-abdominal Infections
• Empiric Therapy for Febrile Neutropenic Patients.
Arapime is also used to associated treatment for these conditions: Bacterial Infections, Complicated Intra-Abdominal Infections, Complicated Urinary Tract Infection, Febrile Neutropenia, Meningitis, Bacterial, Pyelonephritis, Severe Pneumonia, Uncomplicated Urinary Tract Infections, Moderate Pneumonia, Uncomplicated skin and subcutaneous tissue bacterial infections
How Arapime works
Cephalosporins are bactericidal and have the same mode of action as other beta-lactam antibiotics (such as penicillins). Cephalosporins disrupt the synthesis of the peptidoglycan layer of bacterial cell walls. The peptidoglycan layer is important for cell wall structural integrity, especially in Gram-positive organisms. The final transpeptidation step in the synthesis of the peptidoglycan is facilitated by transpeptidases known as penicillin binding proteins (PBPs).
Dosage
Arapime dosage
Recommended dosage schedule for adults with normal renal function
Type of Infection Dose Frequency Duration (Days)
Moderate to severe Pneumonia 1-2 g IV q12h 10
Empiric Therapy for Febrile Neutropenic Patients 2 g IV q8h 7
Mild to moderate Uncomplicated or Complicated Urinary 0.5-1 g IV/IM q12h 7-10
Tract Infections (including pyelonephritis)
Severe Uncomplicated or Complicated Urinary 2 g IV q12h 10
Tract Infections (including pyelonephritis)
Moderate to severe Uncomplicated Skin and Skin Structure 2 g IV q12h 10
Infections
Complicated Intra-abdominal Infections 2 g IV q12h 7-10
Pediatric Patients (2 months up to 16 years)
The maximum dose for pediatric patients should not exceed the recommended adult dose.
Type of Infection Pediatric patients up to 40 kg in weight
Dose Frequency Duration
(Days)
Uncomplicated and Complicated Urinary Tract Infections 50 mg/kg q12h 7-10
(including pyelonephritis)
Uncomplicated Skin and Skin Structure Infections 50 mg/kg q12h 10
Pneumonia 50 mg/kg q12h 10
Febrile Neutropenic Patients 50 mg/kg q8h 7
Impaired Hepatic Function - No adjustment is necessary for patients with impaired hepatic function.
Impaired Renal Function - In patients with impaired renal function (creatinine clearance <60 ml/min), the dose of Arapime should be adjusted. The recommended initial dose of Arapime should be the same as in patients with normal renal function except in patients undergoing hemodialysis. The recommended doses of Arapime in patients with renal insufficiency are presented in the following table:
Creatinine Clearance Recommended Maintenance Schedule
(ml/min)
>60 500 mg q12h 1g q12h 2g q12h 2g q8h
Normal recommended
dosing schedule
30-60 500 mg q24h 1g q24h 2g q24h 2g q12h
11-29 500 mg q24h 500 mg q24h 1g q24h 2g q24h
<11 250 mg q24h 250 mg q24h 500 mg q24h 1g q24h
CAPD 500 mg q48h 1g q48h 2g q48h 2g q48h
Hemodialysis 1g on day 1, then 500 mg q24h thereafter 1g q24h
Preparation of Solutions of Arapime Hydrochloride
Single-dose vial Administration Amount of diluent to be added
500 mg IM 1.3 ml
500 mg IV 5 ml
1 gm IM 2.4 ml
1 gm IV 10 ml
These solutions may be stored up to 24 hours at room temperature or 7 days in a refrigerator.
Arapime Hydrochloride is compatible at concentrations between 1 and 40 mg/ml with the following IV infusion fluids: (1) 0.9% Sodium chloride, (2) 5% and 10% Dextrose.
IV infusion: Add 5 mL, 10 mL, or 10 mL of a compatible IV soln to a vial labeled as containing 500 mg, 1 g, or 2 g, respectively, to provide soln containing approx 100 mg/mL, 100 mg/mL, or 160 mg/mL of the drug, respectively. The appropriate dose of the drug should then be added to a compatible IV soln.
IM inj: Add 1.3 mL or 2.4 mL of an appropriate diluent (e.g. sterile water for inj, NaCl 0.9%) to a vial labeled as containing 500 mg or 1 g respectively, to provide a soln containing approx 280 mg/mL.
Side Effects
Generally Arapime is well tolerated. However, few side-effects including rash, pruritus, urticaria, fever, headache, nausea, vomiting, diarrhea, dizziness, oral moniliasis may occur.
Toxicity
Symptoms of overdose include seizures, encephalopathy, and neuromuscular excitability.
Precaution
In patients with impaired renal function (creatinine clearance <60 ml/min), the dose of Arapime should be adjusted. Arapime should be prescribed with caution in individuals with a history of gastrointestinal diseases, particularly colitis.
Interaction
Increased potential for nephrotoxicity and ototoxicity of aminoglycosides. Increased risk of nephrotoxicity with potent diuretics (e.g. furosemide).
Food Interaction
No interactions found.Arapime Drug Interaction
Moderate: furosemide, furosemideUnknown: ciprofloxacin, ciprofloxacin, apixaban, apixaban, sodium chloride, sodium chloride, acetaminophen, acetaminophen, pantoprazole, pantoprazole, acetaminophen, acetaminophen, cyanocobalamin, cyanocobalamin, cholecalciferol, cholecalciferol, ondansetron, ondansetron
Arapime Disease Interaction
Major: colitisModerate: renal dysfunction, dialysis, liver disease, seizure disorders
Volume of Distribution
- 18.0 ±2.0 L
- 0.3 ±0.1 L/kg [Pediatric]
Elimination Route
The absolute bioavailability of cefepime after an IM dose of 50 mg/kg was 82.3 (±15)% in eight patients.
Half Life
2.0 (± 0.3) hours in normal patients. The average half-life in patients requiring hemodialysis was 13.5 (± 2.7) hours and in patients requiring continuous peritoneal dialysis was 19.0 (± 2.0) hours.
Clearance
- 120 mL/min [Healthy adult male receiving a single 30-minute IV infusions of cefepime]
- 3.3 +/-1.0 mL/min/kg [Petriatic patients (2 months – 11 years of age) receiving a single IV dose]
Elimination Route
Elimination of cefepime is principally via renal excretion with an average (±SD) half-life of 2 (±0.3) hours and total body clearance of 120 (±8) mL/min in healthy volunteers. Arapime is excreted in human milk.
Pregnancy & Breastfeeding use
Pregnancy: There are no adequate and well-controlled studies of Arapime use in pregnant women. Arapime should be used during pregnancy only if clearly needed.
Lactation: Arapime is excreted in human breast milk in very low concentrations. Caution should be exercised when Arapime is administered to a nursing woman.
Contraindication
Hypersensitivity to cefepime or other cephalosporins.
Acute Overdose
Patients who receive an overdose should be carefully observed and given supportive treatment. Symptoms of overdose include encephalopathy (disturbance of consciousness including confusion, hallucinations, stupor, and coma), myoclonus, seizures, and neuromuscular excitability.
Interaction with other Medicine
Renal function should be monitored carefully if high doses of aminoglycosides are to be administered with Arapime because of the increased potential of nephrotoxicity and ototoxicity of aminoglycoside antibiotics. Nephrotoxicity has been reported following concomitant administration of other cephalosporins with potent diuretics such as furosemide.
Storage Condition
Arapime Hydrochloride should be stored in a cool & dry place and protected from light.
Innovators Monograph
You find simplified version here Arapime
Arapime contains Cefepime see full prescribing information from innovator Arapime Monograph, Arapime MSDS, Arapime FDA label
FAQ
What is Arapime used for?
Arapime is a fourth-generation cephalosporin antibiotic. Arapime has an extended spectrum of activity against Gram-positive and Gram-negative bacteria, with greater activity against both types of organism than third-generation agents. Arapime also used in the treatment of various bacterial infections caused by susceptible bacteria, such as pneumonia, urinary tract infections, and skin infections.
How safe is Arapime?
The safety profile of Arapime is excellent and comparable to that of Arapime and those reported for other cephalosporins.
How does Arapime work?
Arapime works by killing bacteria or preventing their growth.
What are the common side effects of Arapime?
Common side effects of Arapime are include:
- Abdominal or stomach cramps
- back, leg, or stomach pains
- bleeding gums, nosebleeds
- confusion
- convulsions
- dark urine
- difficulty with breathing
- fever, chills
- general body swelling
- headache
- irregular heartbeats
- loss of appetite
- mood or mental changes
- muscle cramps in the hands, arms, feet, legs, or face
- nausea or vomiting
- numbness and tingling around the mouth, fingertips, or feet
- tremor
- yellowing of the eyes or skin
Is Arapime safe during pregnancy?
Arapime should be used during pregnancy only if clearly needed. The Arapime group is generally considered safe for use during pregnancy, but each drug is slightly different and may have different side effects.
Is Arapime safe during breastfeeding?
Arapime is acceptable in nursing mothers.
Can I drink alcohol with Arapime?
Using alcohol with certain medicines may also cause interactions to occur.
Can I drive after taking Arapime?
Arapime generally does not cause any problems with your ability to drive a car or operate machinery.
When should be best taken of Arapime?
Arapime are supposed to be taken on an empty stomach should be taken about an hour before a meal, or 2 hours after a meal.
How should be taken of Arapime ?
Arapime injection can also be given intramuscularly. It is usually given every 8 or 12 hours for 7 to 10 days. A healthcare provider can teach you how to properly use the medication by yourself.
How long does Arapime take to work?
Arapime takes about six to eight hours for food to pass through your stomach and small intestine.
What is the half-life of Arapime?
The half-life of Arapime was approximately 2.3 hours.
Can Arapime cause kidney failure?
Patients with renal failure who are treated with Arapime has been reported sporadically.
Who should not take Arapime ?
You should not use this Arapime if you are allergic to Arapime or other cephalosporin antibiotic.
What happens if I miss a dose?
Use the Arapime as soon as you can, but skip the missed dose if it is almost time for your next dose. Do not use two doses at one time.
Can I take Arapime for a long time?
Continue to use this Arapime for the full time prescribed, even if symptoms disappear after a few days. Stopping the Arapime too early may result in a return of the infection.
Is Arapime bad for liver?
Arapime is considered well-tolerated and is associated with few adverse reactions. Although Arapime -induced neurotoxicity and nephrotoxicity have been reported in recent years, there are currently no formal reports of hepatic injury caused by this Arapime.
How long can I take Arapime?
Use this Arapime for the full prescribed length of time, even if your symptoms quickly improve. Some infections must be treated for up to 6 weeks.
Can I overdose on Arapime?
Arapime related neurological toxicity has been associated with overdosing due to severe renal dysfunction.
How often can I take Arapime?
Arapime is usually given every 8 or 12 hours for 7 to 10 days.
What happens if I miss a dose?
Use the medicine as soon as you can, but skip the missed dose if it is almost time for your next dose. Do not use two doses at one time.