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» Home » Drug Database » Antifungal Drugs » Echinocandins » caspofungin
Brand Name :
No Data Available.
country | status | Month | Year |
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Synonyms :
caspofungin
Class :
Antifungals, Echinocandin
Actions and spectrum:
caspofungin is an antifungal medication that belongs to the class of echinocandins. It is used to treat invasive fungal infections caused by Aspergillus and Candida species. caspofungin works by inhibiting the synthesis of beta (1,3)-D-glucan, a major component of fungal cell walls, resulting in weakening and eventual death of the fungal cell.
caspofungin is only effective against certain types of fungi and is not recommended for the treatment of non-fungal infections. It is typically used in patients who are unable to tolerate or have failed other antifungal therapies.
No drug interaction found for caspofungin and .
may diminish the serum concentration when combined with caspofungin
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may decrease the therapeutic effect of Antifungal Agents when combined
may decrease the therapeutic effect of Antifungal Agents when combined
may decrease the therapeutic effect of Antifungal Agents when combined
may decrease the therapeutic effect of Antifungal Agents when combined
may decrease the therapeutic effect of Antifungal Agents when combined
may increase the levels of serum concentration of ivacaftor/tezacaftor
may enhance the serum concentration
may enhance the serum concentration
may enhance the serum concentration
may enhance the serum concentration of CYP3A4 inhibitors
may enhance the serum concentration of CYP3A4 inhibitors
may enhance the serum concentration of CYP3A4 inhibitors
may enhance the serum concentration when combined with nifedipine
may increase the serum concentration of abemaciclib
may increase the level of serum concentration of adagrasib
may increase or decrease the activity of this enzyme when combined with sparsentan
May enhance the serum concentration when combined with levomilnacipran
may enhance the serum concentration when combined with upadacitinib
may have an increased adverse effect when combined with caspofungin
may enhance the serum concentration when combined with tolvaptan
It may enhance serum concentration when combined with CYP3A4 Inhibitors (Moderate)
CYP3A4 Inhibitors (Moderate) may increase the serum concentration when combined with Zanubrutinib
rifampin: they may diminish the serum concentration of caspofungin
may enhance the serum concentration when combined
may enhance the concentration of serum when combined with ubrogepant
may enhance the serum concentrations of the active metabolites
may enhance the serum concentration of ubrogepant
may diminish the metabolism of cyclosporine
may enhance the serum concentration when combined
may enhance the concentration of serum when combined with istradefylline
may enhance the concentration of serum when combined with alfentanil
may enhance the concentration of serum when combined with astemizole
may enhance the concentration of serum when combined with avanafil
may enhance the concentration of serum when combined with brigatinib
may enhance the concentration of serum when combined with bromocriptine
budesonide inhaled/formoterol/glycopyrrolate inhaled
may enhance the concentration of serum when combined with budesonide
may enhance the concentration of serum when combined with cilostazol
may enhance the concentration of serum when combined with cisapride
may enhance the concentration of serum when combined with cobimetinib
may enhance the concentration of serum when combined with colchicine
may enhance the concentration of serum when combined with dapoxetine
may enhance the concentration of serum when combined with daridorexant
may enhance the concentration of serums when combined with deflazacort
may enhance the concentration of serum when combined with eliglustat
may enhance the concentration of serum when combined with encorafenib
may enhance the concentration of serum when combined with entrectinib
may enhance the concentration of serum when combined with eplerenone
may enhance the concentration of serum when combined with fentanyl
may enhance the concentration of serum when combined with guanfacine
may enhance the concentration of serum when combined with ibrutinib
may enhance the concentration of serum when combined with elacestrant
may enhance the QTc-prolonging effect of each other when combined
lurasidone: they may enhance the serum concentration of CYP3A4 Inhibitors
CYP3A4 Inhibitors: they may enhance the serum concentration of mavacamten
may increase the levels of serum concentration of ergot derivatives
they decrease the concentration of active metabolites of roflumilast in the serum
it increases the concentration of CYP3A4 substrates in the serum
it increases the concentration of CYP3A4 substrates in serum
may increase the levels of serum concentration of eletriptan
may increase the serum concentration of acalabrutinib
CYP3A4 inhibitors increase the concentration of active metabolites of simvastatin in the serum
may enhance the serum concentration of simeprevir
may enhance the serum concentration
may enhance the serum concentration of fostemsavir
may enhance the serum concentrations of flibanserin
may decrease the therapeutic effect when combined with saccharomyces boulardii
may diminish the serum concentration when combined with nintedanib
CYP3A4 Inhibitors (Moderate) may increase the serum concentration when combined with Sertindole
CYP3A4 Inhibitors (Moderate) may decrease serum concentrations when combined with the active metabolite(s) when combined with Infigratinib
CYP3A4 Inhibitors (Moderate) may increase the serum concentration when combined with methysergide
CYP3A4 Inhibitors (Moderate) may increase the serum concentration when combined with Pacritinib
may decrease the therapeutic effect when combined with progesterone
may enhance serum concentrations of the active metabolites
may enhance the serum concentration when combined
may enhance the concentration of serum when combined with pimozide
The serum concentration of alfuzosin can be increased by strong CYP3A4 inhibitors
OATP1B1/1B3 (SLCO1B1/1B3) inhibitors increase the concentration of asunaprevir in the serum
OATP1B1/1B3 (SLCO1B1/1B3) inhibitors increase the concentration of elbasvir and grazoprevir in the serum
BCRP/ABCG2 inhibitors increase the concentration of pazobanib in the serum
OATP1B1/1B3 (SLCO1B1/1B3) inhibitors increase the concentration of taurursodiol in the serum
OATP1B1/1B3 (SLCO1B1/1B3) inhibitors increase the concentration of voxilaprevir in the serum
may enhance the serum concentration when combined
may diminish the concentration of serum when combined with CYP3A4 substrates
may enhance the concentration of serum when combined with ergot derivatives
may enhance the concentration of serum when combined with ergot derivatives
may enhance the concentration of serum when combined with aprepitant
may enhance the concentration of serum when combined with asunaprevir
may enhance the concentration of serum when combined with bosutinib
may enhance the concentration of serum when combined with budesonide
may enhance the concentration of serum when combined with isavuconazonium sulfate
may enhance the concentration of serum when combined with domperidone
may enhance the concentration of serum when combined with fosaprepitant
may enhance the concentration of serum when combined with ivabradine
may increase the serum concentration of each other when combined
it increases the concentration of OATP1B1/1B3 substrates in the serum
CYP3A4 inhibitors (Strong) may increase the serum concentration of estrogen related drugs
bazedoxifene/conjugated estrogens
CYP3A4 inhibitors (Strong) may increase the serum concentration of estrogen related drugs
CYP3A4 inhibitors (Strong) may increase the serum concentration of estrogen related drugs
synthetic conjugated estrogens, a
CYP3A4 inhibitors (Strong) may increase the serum concentration of estrogen related drugs
synthetic conjugated estrogens, b
CYP3A4 inhibitors (Strong) may increase the serum concentration of estrogen related drugs
may increase the serum concentration of ergot derivatives
may increase the serum concentration of ergot derivatives
may increase the serum concentration of ergot derivatives
may increase the serum concentration of ergot derivatives
may increase the serum concentration of ergot derivatives
may increase the levels of serum concentration of estrogen derivatives
may increase the levels of serum concentration of estrogen derivatives
bazedoxifene/conjugated estrogens
may increase the levels of serum concentration of estrogen derivatives
may increase the levels of serum concentration of estrogen derivatives
may increase the levels of serum concentration of estrogen derivatives
may increase the levels of serum concentration of hormonal contraceptives
may increase the levels of serum concentration of hormonal contraceptives
may increase the levels of serum concentration of hormonal contraceptives
may increase the levels of serum concentration of hormonal contraceptives
synthetic conjugated estrogens, a
may increase the serum concentration
synthetic conjugated estrogens, b
may increase the serum concentration
may increase the serum concentration
may increase the QTc-prolonging effect
may increase the QTc-prolonging effect
may increase the QTc-prolonging effect
may increase the QTc-prolonging effect
may increase the QTc-prolonging effect
may increase the levels of serum concentrations
may increase the levels of serum concentrations
may increase the levels of serum concentrations
may increase the levels of serum concentrations
may increase the levels of serum concentrations
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
acetaminophen and phenyltoloxamine
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
acetaminophen and phenyltoloxamine
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
may increase the levels of serum concentration
may enhance the levels of serum concentration
may enhance the levels of serum concentration
may enhance the levels of serum concentration
may enhance the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
it increases the concentration of CYP3A4 substrates in the serum
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
it increases the concentration of CYP3A4 substrates in the serum
hydrocodone/chlorpheniramine/pseudoephedrine
may diminish the serum concentration
it increases the concentration of alosetron in the serum
they decrease the concentration of linagliptin in the serum
may increase the serum concentration of clozapine
may increase the levels of serum concentrations of cariprazine
may enhance the serum concentration
may increase the serum concentration of zopiclone
may enhance the serum concentration of CYP3A4 inhibitor
may increase the toxic effect of opioid agonists
may enhance the serum concentration
may diminish serum concentrations when combined with doxercalciferol
may enhance the serum concentrations
may increase the level of serum concentration of itraconazole
CYP3A4 inhibitors increase the concentration of finerenone in the serum
CYP3A4 inhibitors increase the concentration of tacrolimus in the serum
may increase the serum concentration of pimecrolimus
may increase the serum concentration
may reduce the effect of zavegepant
may enhance the serum concentration of dexamethasone
may increase the QTc prolonging effect of QTc prolonging agents
may decrease the therapeutic effect of Amphotericin B
CYP3A4 Inhibitors (Moderate) may increase the serum concentration when combined with Vilazodone
It may enhance serum concentration when combined with CYP3A4 Inhibitors (Moderate)
It may enhance serum concentration when combined with CYP3A4 Inhibitors (Moderate)
It may increase serum concentration when combined with CYP3A4 Inhibitors (Moderate)
It may enhance the serum concentration when combined with CYP3A4 Inhibitors (Moderate)
It may increase the serum concentration when combined with CYP3A4 Inhibitors (Moderate)
It may enhance the serum concentration when combined with CYP3A4 Inhibitors (Moderate)
It may enhance the serum concentration when combined with CYP3A4 Inhibitors (Moderate)
It may enhance the serum concentration when combined with CYP3A4 Inhibitors (Moderate)
It may enhance the serum concentration when combined with CYP3A4 Inhibitors (Moderate)
It may enhance the serum concentration when combined with CYP3A4 Inhibitors (Moderate)
It may enhance the serum concentration when combined with CYP3A4 Inhibitors (Moderate)
It may enhance the serum concentration when combined with CYP3A4 Inhibitors (Moderate)
It may enhance the serum concentration when combined with CYP3A4 Inhibitors (Moderate)
may enhance the serum concentration when combined with ziprasidone
methylprednisolone hemisuccinate
may increase the levels of serum concentration
may decrease the levels of serum concentration
It may enhance the serum concentration when combined with dexamethasone
may enhance the concentration of serum when combined with alprazolam
may enhance the concentration of serum when combined with carbamazepine
may enhance the concentration of serum when combined with cyclosporine
may enhance the concentration of serum when combined with dofetilide
may enhance the concentration of serum when combined with ixabepilone
may enhance the concentration of serum when combined with midazolam
may enhance the concentration of serum when combined with nimodipine
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
bazedoxifene/conjugated estrogens
may increase the levels of serum concentration
synthetic conjugated estrogens, a
may increase the levels of serum concentration
synthetic conjugated estrogens, b
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
buprenorphine,long-acting injection
may enhance the serum concentration of Buprenorphine
may enhance the concentration of serum when combined with sirolimus
It may enhance the serum concentration when combined with CYP3A4 Inhibitors
The serum concentration of amlodipine can be increased by strong inhibitors of CYP3A4
The use of strong CYP3A4 inhibitors may elevate the serum concentration of benidipine
it may increase the levels of serum concentration
it may increase the levels of serum concentration
it may increase the levels of serum concentration
it may increase the levels of serum concentration
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
it may increase the levels of serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates
may enhance the serum concentration when combined with dexamethasone
fusidic acid and betamethasone
may enhance the serum concentration when combined
may enhance the concentration of serum when combined with alitretinoin
may enhance the concentration of serum when combined with amiodarone
may decrease the therapeutic effect when combined with amphotericin b
may enhance the concentration of serum when combined with aripiprazole
may enhance the concentration of serum when combined with aripiprazole lauroxil
may enhance the concentration of serum when combined with atogepant
may enhance the concentration of serum when combined with atorvastatin
may enhance the concentration of serum when combined with avacopan
may enhance the concentration of serum when combined with axitinib
may enhance the concentration of serums when combined with bedaquiline
may enhance the concentration of serum when combined with benzhydrocodone
may enhance the concentration of serum when combined with bortezomib
may enhance the concentration of serum when combined with brexpiprazole
may enhance the concentration of serum when combined with buprenorphine
may enhance the serum concentration when combined
may enhance the serum concentration when combined
may diminish the serum concentration of each other when combined
may enhance the concentration of serum when combined with methylprednisolone
framycetin, dexamethasone, and gramicidin
may enhance the serum concentration when combined
may have an increased QTc-prolonging effect when combined with QT-prolonging agents
may have an increased QTc-prolonging effect when combined with QT-prolonging agents
may have an increased QTc-prolonging effect when combined with QT-prolonging agents
may have an increased QTc-prolonging effect when combined with QT-prolonging agents
may have an increased QTc-prolonging effect when combined with QT-prolonging agents
CYP3A4 inhibitors increase the concentration of sirolimus in the serum
CYP3A4 inducers increase the concentration of buspirone in the serum
almotriptan serum concentration may also be increased by CYP3A4 inhibitors (strong)
Dosage Forms & Strengths
powder for injection
70mg/vial
50mg/vial
(Off-label):
Indicated for initial treatment of Candida auris infections, recommended by the CDC:
Day-1 initial dose: Infusion of 70 mg /m² intravenous
Day 2 and later: 50 mg/m² Intravenous every Day
Indicated for Invasive Aspergillosis :
Day-1 initial dose: Infusion of 70 mg intravenously over one hour (as a single dose)
Maintenance: 50 mg Intravenous infused every one hour, every day
Dosage Forms & Strengths
powder for injection
70mg/vial
50mg/vial
(Off-label) :
Neonates and infants below 2 months
25 mg/m²/day intravenous
Above 2 months
Day-1 initial dose: 70 mg/m² Intravenous
Day 2 and later: 50 mg/m² Intravenous every Day
Dose Adjustments
Coadministration with CYP inducers: 70 mg/m² intravenous every Day, should not exceed more than 70 mg every Day
Hepatic impairment: Safety and efficacy is not established
Refer to the adult dosing regimen.
Frequency defined
>10%
Increased transaminases (2-18%)
Respiratory failure (2-20%)
Hypotension (3-20%)
Rash (4-23%)
Diarrhoea (6-27%)
Fever (6-30%)
Shivering (9-23%)
enhanced serum alkaline phosphatase levels (9-22%)
Septic shock (11% to 14%)
Infused vein complications/ phlebitis (20-35%)
1-10%
Pleural effusion (9%)
Abdominal pain
Respiratory distress (up to 8%)
Nausea
Anemia
Neutropenia
Hypokalemia
Erythema
Hematuria
Increased serum creatinine
Myalgia
Paresthesia
Sepsis
Vomiting
Decreased Hgb
Chills
Dizziness
Facial edema, flushing
Hyperbilirubinemia
Induration
Pain
Pruritus
Tachycardia
<1%
Erythema multiforme
Pancreatitis
Liver failure
Nephrotoxicity
Stevens-Johnson syndrome
Hepatic necrosis
Anaphylaxis
Renal impairment
Post marketing Reports
lymphatic system and blood disorders: coagulopathy, neutropenia, Anemia, febrile neutropenia, thrombocytopenia.
Cardiac disorders: atrial fibrillation, cardiac arrest, tachycardia, Arrhythmia, bradycardia, myocardial infarction.
Gastrointestinal disorders: abdominal pain upper, dyspepsia, Abdominal distension, constipation.
General disorders: Asthenia, infusion site swelling/pain/pruritus, peripheral edema, fatigue.
Infections and infestations: sepsis, Bacteremia, urinary tract infection.
Nutrition and metabolic disorders: decreased appetite, hypomagnesemia, hyperglycemia, Anorexia, fluid overload, hypercalcemia, hypokalemia.
Nervous system disorders: dizziness, tremor, Convulsion, somnolence.
Urinary and Renal disorders: renal failure, Hematuria.
subcutaneous tissue and Skin disorders: petechiae, skin exfoliation, Erythema, skin lesion, urticaria.
Hepatobiliary disorders: hepatomegaly, hyperbilirubinemia, Hepatic failure, hepatotoxicity, jaundice.
Musculoskeletal, bone and connective tissue disorders: back pain, Arthralgia, pain in extremity.
Psychiatric disorders: confusional state, insomnia, Anxiety, depression.
Respiratory, mediastinal, and thoracic disorders: epistaxis, tachypnea, Dyspnea, hypoxia.
Vascular disorders: hypertension, Flushing, phlebitis
Black Box Warning:
caspofungin does not have any black box warning.
Contraindication/Caution:
Contraindication:
caspofungin is contraindicated in patients with a history of hypersensitivity to caspofungin acetate or any component of the formulation. It should also not be co-administered with drugs that are known to have a potential for hepatotoxicity, such as amphotericin B, aminoglycosides, or other hepatotoxic drugs. Additionally, caspofungin should not be used for the treatment of infections caused by Cryptococcus or Zygomycetes fungi.
Caution:
comorbidities
caspofungin is well-tolerated and can be used in patients with comorbidities such as liver and kidney impairment, although dose adjustments may be required. However, caution should be exercised when using caspofungin in patients with hypersensitivity to echinocandins, as well as in patients with a history of severe allergic reactions to other medications. caspofungin should also be used with caution in patients with a history of hepatotoxicity or liver disease.
Pregnancy consideration: pregnancy category C
Lactation: safety and efficacy not established
Pregnancy category:
Pharmacology:
caspofungin is an antifungal drug that belongs to the echinocandin class of drugs. It works by inhibiting the synthesis of β-(1,3)-D-glucan, one of the major components of the fungal cell wall. This inhibition leads to osmotic instability, causing cell death in susceptible fungi. caspofungin has activity against a broad spectrum of fungal pathogens, including Candida species, Aspergillus species, and some rare molds.
Pharmacodynamics:
caspofungin is an antifungal drug that belongs to the echinocandin class. It works by inhibiting the synthesis of beta-(1,3)-D-glucan, one of the major components of the fungal cell wall. This leads to the weakening of the cell wall and subsequent fungal cell death. caspofungin has activity against a broad range of fungi, including Candida species, Aspergillus species, and some other rare fungal species.
caspofungin is a fungicidal agent, meaning that it kills the fungal cells rather than just inhibiting their growth. caspofungin has a broad spectrum of activity against many clinically important fungi, including those that are resistant to other antifungal drugs such as fluconazole or itraconazole.
Pharmacokinetics:
Absorption
caspofungin is administered by intravenous infusion and therefore does not undergo absorption through the gastrointestinal tract.
Distribution
After administration, caspofungin is widely distributed throughout the body, with a volume of distribution of approximately 0.2 L/kg
Metabolism
caspofungin is not extensively metabolized, and the liver is the primary site of elimination. caspofungin is metabolized by hydrolysis and N-acetylation to inactive metabolites.
Elimination and excretion
The elimination half-life of caspofungin is 9-11 hours, and steady-state concentrations are reached after the third dose. caspofungin does not undergo significant hepatic metabolism or renal excretion and is eliminated through biliary excretion.
Administration:
caspofungin is administered intravenously (IV) by a healthcare provider in a hospital setting. It is usually given once a day, and the dosage depends on various factors such as the patient’s age, weight, and medical condition.
The infusion should be given over approximately one hour, and the injection site should be monitored for possible infusion-related reactions. It is important to follow the healthcare provider’s instructions for the proper administration of caspofungin.
Patient information leaflet
Generic Name: caspofungin
Pronounced: [ KAS-poe-FUN-jin ]
Why do we use caspofungin?
caspofungin is one of the antifungal medications that is used to treat Candida auris infections. caspofungin belongs to a class of antifungal medications called echinocandins, which work by inhibiting the synthesis of the fungal cell wall. This prevents the growth and spread of the Candida auris fungus, ultimately leading to its death.
One of the benefits of caspofungin is that it has a broad spectrum of activity against many different types of fungi, including Candida auris. Additionally, studies have shown that caspofungin may be more effective than other antifungal medications, such as fluconazole, in treating Candida auris infections.
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» Home » Drug Database » Antifungal Drugs » Echinocandins » caspofungin
Brand Name :
No Data Available.
country | status | Month | Year |
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Synonyms :
caspofungin
Class :
Antifungals, Echinocandin
Dosage Forms & Strengths
powder for injection
70mg/vial
50mg/vial
(Off-label):
Indicated for initial treatment of Candida auris infections, recommended by the CDC:
Day-1 initial dose: Infusion of 70 mg /m² intravenous
Day 2 and later: 50 mg/m² Intravenous every Day
Indicated for Invasive Aspergillosis :
Day-1 initial dose: Infusion of 70 mg intravenously over one hour (as a single dose)
Maintenance: 50 mg Intravenous infused every one hour, every day
Dosage Forms & Strengths
powder for injection
70mg/vial
50mg/vial
(Off-label) :
Neonates and infants below 2 months
25 mg/m²/day intravenous
Above 2 months
Day-1 initial dose: 70 mg/m² Intravenous
Day 2 and later: 50 mg/m² Intravenous every Day
Dose Adjustments
Coadministration with CYP inducers: 70 mg/m² intravenous every Day, should not exceed more than 70 mg every Day
Hepatic impairment: Safety and efficacy is not established
Refer to the adult dosing regimen.