Epomax

Epomax may be available in the countries listed below.

Ingredient matches for Epomax

Epoetin Alfa

Epoetin Alfa is reported as an ingredient of Epomax in the following countries:

• Slovenia

International Drug Name Search

Perindopril-Teva

Perindopril-Teva may be available in the countries listed below.

Ingredient matches for Perindopril-Teva

Perindopril

Perindopril erbumine (a derivative of Perindopril) is reported as an ingredient of Perindopril-Teva in the following countries:

• Switzerland

International Drug Name Search

Dalteparin Sodium

Class: Heparins
Chemical Name: Heparin, sodium salt
CAS Number: 9041-08-1
Brands: Fragmin

• 
  

  Epidural or spinal hematomas and neurologic injury, including long-term or permanent paralysis, associated with concurrent use of low molecular weight (LMW) heparins or heparinoids and neuraxial (spinal/epidural) anesthesia or spinal puncture.^{1 35 77}

  
  


• 
  

  Risk increased by use of indwelling epidural catheters or by concomitant use of drugs affecting hemostasis (e.g., NSAIAs, platelet inhibitors, other anticoagulants).^{1 35 77 78}

  
  


• 
  

  Risk also increased by traumatic or repeated epidural or spinal puncture.^{1 35}

  
  


• 
  

  Monitor frequently for signs and symptoms of neurologic impairment and treat urgently if neurologic compromise noted.^{1 35 77 78}

  
  


• 
  

  Consider potential benefits versus risks of spinal or epidural anesthesia or spinal puncture in patients receiving or being considered for thromboprophylaxis with anticoagulants.^{1 35} (See Neurologic Effects under Cautions.)

  
  

Introduction

Anticoagulant; a low molecular weight heparin.^{1 3 5 10 22 23 26}

Uses for Dalteparin Sodium

Unstable Angina and Non-ST-Segment Elevation/Non-Q-Wave MI

Reduction in the risk of acute cardiac ischemic events (death and/or MI) in patients with unstable angina or non-ST-segment elevation/non-Q-wave MI (i.e., non-ST-segment elevation acute coronary syndromes).^{1 49 51 52 53 54 66 103 104 105 106} Used concurrently with aspirin and/or other standard therapy (e.g., nitrates, β-adrenergic blockers, clopidogrel, platelet glycoprotein [GP] IIb/IIIa-receptor inhibitors) in such patients.^{1 49 51 52 53 54 66 103 104 105 106 121}

ACC, AHA, and other clinicians prefer an LMW heparin over unfractionated heparin in patients with non-ST-segment elevation acute coronary syndromes unless renal failure is present or CABG is planned within 24 hours.^{105 121}

Based on limited data, the ACC, AHA, and other experts consider the use of an LMW heparin to be a reasonable alternative to unfractionated heparin in patients with non-ST-segment elevation acute coronary syndromes undergoing PCI.⁹⁴

Hip-Replacement Surgery

Prophylaxis of postoperative DVT and pulmonary embolism in patients undergoing hip-replacement surgery.^{1 27 60 63 64 73 90 118}

Consider extended prophylaxis† in patients undergoing hip-replacement surgery who have ongoing risk factors for venous thromboembolism (e.g., obesity, delayed mobilization, cancer, history of venous thromboembolism).¹¹⁸

Hip-Fracture Surgery

An LMW heparin recommended by American College of Chest Physicians (ACCP) for prophylaxis of postoperative DVT and pulmonary embolism in patients undergoing hip-fracture surgery†.¹¹⁸

Consider extended prophylaxis† in patients undergoing hip-fracture surgery† who have ongoing risk factors for venous thromboembolism (e.g., obesity, delayed mobilization, cancer, history of venous thromboembolism).¹¹⁸

Knee-Replacement Surgery

Routine thromboprophylaxis with an LMW heparin recommended by ACCP in patients undergoing knee-replacement surgery†.¹¹⁸

Knee Arthroscopy

An LMW heparin suggested by ACCP based on limited data for prophylaxis of venous thromboembolism in high-risk patients undergoing knee arthroscopy† (e.g., those with preexisting thromboembolic risk factors or following a prolonged or complicated procedure).¹¹⁸

General Surgery

Prophylaxis of postoperative venous thromboembolism in patients undergoing general (e.g., abdominal, gynecologic, urologic) surgery who are at risk for thromboembolic complications.^{1 3 6 7 8 9 10 19 20 21 22 90 118}

Early ambulation without specific thromboprophylaxis recommended by ACCP in patients undergoing general surgery who are at low risk for venous thromboembolism (those undergoing minor operations who are <40 years of age and who have no clinical risk factors).^{27 90 118}

Recommended as alternative to fixed low-dose unfractionated heparin in moderate-risk general surgery patients (those undergoing nonmajor surgery who are 40–60 years of age or who have additional risk factors for thromboembolism, patients <40 years of age undergoing major surgery with no additional risk factors, and patients with risk factors who are undergoing minor surgery).^{90 118}

Recommended as alternative to fixed low-dose unfractionated heparin in patients undergoing general surgery who are at higher risk for thromboembolism (those undergoing major surgery who are >40 years of age or who have additional risk factors and patients undergoing nonmajor surgery who are >60 years of age or who have additional risk factors).^{27 90 118}

Recommended as alternative to low-dose unfractionated heparin and in combination with intermittent pneumatic compression or graduated compression stockings^{27 90 118} in high-risk general surgery patients (those >40 years of age with multiple risk factors such as a history of previous venous thromboembolism, cancer, or a hypercoagulable state).^{27 90} Continue LMW heparin after hospital discharge in selected high-risk general surgery patients, including those undergoing major cancer surgery.^{90 118}

Thromboprophylaxis with low-dose unfractionated heparin, LMW heparin, intermittent pneumatic compression, graduated compression stockings, or a combination of these interventions suggested in patients undergoing laparoscopic gynecologic procedures who have additional risk factors for venous thromboembolic events (e.g., malignancy, older age, previous thromboembolism, prior pelvic radiation therapy, use of an abdominal surgical approach).¹¹⁸

Thromboprophylaxis with LMW heparin recommended as alternative to low-dose unfractionated heparin^{1 60 104} or intermittent pneumatic compression in patients undergoing major gynecologic surgery for benign disease who do not have additional risk factors for thromboembolism.¹¹⁸ Begin just prior to surgery and continue until hospital discharge or patient is ambulatory.¹¹⁸

Routine prophylaxis with LMW heparin or unfractionated heparin recommended in patients undergoing extensive gynecologic procedures for malignancy and in those with additional risk factors for venous thromboembolic events.¹¹⁸ Alternative regimens include intermittent pneumatic compression continued until hospital discharge, or the combination of low-dose unfractionated heparin or LMW heparin and intermittent pneumatic compression or graduated compression stockings.¹¹⁸ Continue extended prophylaxis† for 2–4 weeks following hospital discharge in those at particularly high risk for thromboembolism (e.g., previous cancer surgery, >60 years of age, history of thromboembolism).¹¹⁸

Thromboprophylaxis with an LMW heparin or low-dose unfractionated heparin recommended in patients undergoing major vascular surgery who have additional risk factors for thromboembolism (e.g., advanced age, limb ischemia, long duration of surgery, intraoperative local trauma).¹¹⁸

Medical Conditions Associated with Thromboembolism

Prophylaxis of thromboembolism in medical patients with CHF or severe lung disease or who have severely restricted mobility in conjunction with one or more additional risk factors (e.g., cancer, previous venous thromboembolism, sepsis, acute neurologic disease, inflammatory bowel disease).^{1 90 118 125}

Neurosurgery

An LMW heparin recommended by ACCP as alternative therapy (e.g., instead of intermittent pneumatic compression with or without graduated compression stockings) for prophylaxis of thromboembolism in selected patients undergoing intracranial neurologic surgery†.¹¹⁸

Combination of an LMW heparin or low-dose unfractionated heparin with graduated compression stockings and/or intermittent pneumatic compression recommended in patients with multiple risk factors for venous thromboembolism.¹¹⁸

Elective Spinal Surgery

An LMW heparin recommended by ACCP for prevention of venous thromboembolism in patients undergoing elective spinal surgery† who have additional risk factors (e.g., advanced age, known malignancy, neurologic deficit, previous venous thromboembolic event, anterior surgical approach), as alternative to postoperative low-dose unfractionated heparin or perioperative intermittent pneumatic compression.¹¹⁸

Combine anticoagulant therapy with graduated compression stockings and/or intermittent pneumatic compression in patients with multiple risk factors for venous thromboembolism.¹¹⁸

Acute Spinal Cord Injury

An LMW heparin recommended by ACCP as first-line prophylaxis of thromboembolism in patients with acute spinal cord injury†.¹¹⁸

For prevention of thromboembolism in the rehabilitation phase of acute spinal cord injury†, continue therapy with an LMW heparin or, alternatively, convert to full-dose oral anticoagulation.^{73 118}

Trauma

An LMW heparin recommended by ACCP as first-line prophylaxis of thromboembolism in patients with major trauma†.⁹⁰

Initiate prophylaxis as soon as considered safe to do so and continue until hospital discharge, including during inpatient rehabilitation.^{73 118}

Extended prophylaxis† after hospital discharge suggested in patients with major mobility impairment.¹¹⁸

Burns

An LMW heparin recommended by ACCP as alternative to low-dose unfractionated heparin in burn patients who have at least one additional risk factor for venous thromboembolism (e.g., advanced age, morbid obesity, extensive or lower extremity burns, concomitant lower extremity trauma, use of a femoral catheter, or prolonged immobility).¹¹⁸ Initiate prophylaxis as soon as the risk of bleeding is no longer high, provided no contraindications exist.¹¹⁸

Long-Distance Travel

Single prophylactic dose of an LMW heparin may be considered for thromboprophylaxis prior to travel† as alternative to below-knee graduated compression stockings in those with risk factors for venous thrombosis (e.g., previous DVT, coagulation disorder, limited mobility, current or recent cancer, large varicose veins, severe obesity).¹¹⁸ Data insufficient to support routine use in any group of travelers.¹¹⁸

Acute Ischemic Stroke

An LMW heparin recommended by ACCP as first-line prophylaxis of thromboembolism in patients with acute ischemic stroke† and impaired mobility who have no contraindications.¹²⁰

Thromboembolism Occurring During Pregnancy

An LMW heparin recommended in selected patients for initial treatment and secondary prevention of thromboembolism during pregnancy†.^{88 90 91 96 97 98 99 117 153 154}

Used alone or in combination with aspirin for prevention of pregnancy loss in women with antiphospholipid antibodies (APLAs) and previous pregnancy losses.¹¹⁷

Embolism Associated with Atrial Fibrillation/Flutter

An LMW heparin may be initiated at diagnosis to reduce the incidence of embolism in patients with atrial fibrillation/flutter of <48 hours' duration who are undergoing cardioversion†, provided no contraindications exist.¹¹⁹

Base the need for anticoagulation in such patients on the patient's individual risk of thromboembolism.⁹⁸ In patients requiring immediate cardioversion because of hemodynamic instability, cardioversion should not be delayed for prior initiation of anticoagulation.⁹⁸

An LMW heparin may be substituted for oral anticoagulant (e.g., warfarin) therapy in patients with atrial fibrillation† who require a series of diagnostic or surgical procedures that necessitate interruption of oral anticoagulation for >1 week or in selected high-risk patients who require interruption of oral anticoagulant therapy for shorter periods.⁹⁸ Efficacy of these alternative therapies in this situation uncertain.⁹⁸

Thromboembolism Associated with Prosthetic Heart Valves

An LMW heparin used with follow-up oral anticoagulation (e.g., warfarin) in selected patients for prevention of thromboembolism associated with prosthetic heart valves†.^{88 90 91 96 97 98 99 124}

In patients with prosthetic heart valves in whom therapy with warfarin must be discontinued (e.g., those undergoing major surgery), substitution of an LMW heparin or unfractionated heparin is recommended by ACCP, AHA, and ACC.^{124 153}

ACCP and other clinicians suggest that use of aggressive, adjusted-dose therapy with sub-Q LMW heparin or high-dose sub-Q unfractionated heparin therapy is reasonable in pregnant women with prosthetic mechanical heart valves†.^{88 117 153}

DVT and Pulmonary Embolism

An LMW heparin recommended for treatment of suspected DVT† or acute nonmassive pulmonary embolism† while awaiting confirmation of diagnosis, provided no contraindications exist.^{116 117}

Preferred over unfractionated heparin for treatment of confirmed DVT† or acute nonmassive pulmonary embolism†.¹¹⁶

Recommended by ACCP as alternative to oral anticoagulation (e.g., with warfarin) for long-term treatment of confirmed DVT† or acute nonmassive pulmonary embolism† in patients in whom oral anticoagulation is contraindicated or inconvenient.¹¹⁶

ACCP recommends that unfractionated heparin be substituted for LMW heparin in patients with severe renal failure.¹¹⁶

Superficial Thrombophlebitis

An LMW heparin suggested by ACCP as an alternative to unfractionated heparin for treatment of superficial thrombophlebitis†.¹¹⁶

Systemic Venous Thrombosis in Pediatric Patients

An LMW heparin suggested by ACCP for the treatment and prevention of systemic venous thrombosis in neonates and children†; data insufficient to make strong recommendations in neonates.¹²³

Renal Vein Thrombosis

An LMW heparin suggested by ACCP for the treatment of renal vein thrombosis in neonates†; data limited and use of anticoagulant or thrombolytic therapy is controversial in such patients.¹²³

Cerebral Venous Sinus Thrombosis

An LMW heparin recommended by ACCP with follow-up oral anticoagulation (e.g., warfarin) in adults with acute cerebral venous sinus thrombosis†, even in the presence of hemorrhagic venous infarcts.^{120 154}

Neonates without large ischemic infarction or intracranial hemorrhage: Initial therapy with an LMW heparin or unfractionated heparin suggested, then administer LMW heparin for 3 months.¹²³

Neonates with large infarcts or intracranial hemorrhage: Radiographic monitoring suggested; initiate anticoagulation if extension of thrombus detected.¹²³

Children without major intracranial hemorrhage: LMW heparin or unfractionated heparin followed by LMW heparin or oral anticoagulation (e.g., with warfarin).¹²³

Spontaneous Aortic Thrombosis

Neonates experiencing spontaneous aortic thrombosis with evidence of renal ischemia: Urgent, aggressive use of thrombolytic or surgical therapy supported by anticoagulation with an LMW heparin or unfractionated heparin suggested by ACCP.¹²³

Acute Ischemic Complications Following ST-Segment Elevation MI

AHA, ACC, and ACCP suggest that adjunctive therapy with an LMW heparin may be considered in place of unfractionated heparin as adjunctive therapy for patients ≤75 years of age who have preserved renal function (S_cr ≤2.5 mg/dL in men or ≤2 mg/dL in women).^{145 146}

Most experience to date with enoxaparin as adjunct to tenecteplase in patients with ST-segment elevation MI†; additional study and experience recommended before routine use of LMW heparin instead of unfractionated heparin in such patients.^{145 146 148}

ACC and AHA recommend use of an LMW heparin or unfractionated heparin for prevention of systemic embolism following ST-segment elevation MI† in high-risk patients (e.g., patients with large or anterior MI, atrial fibrillation, previous embolus, documented left ventricular thrombus, cardiogenic shock).¹⁴⁵

Preferred by ACC and AHA over unfractionated heparin for prophylaxis of DVT and pulmonary embolism in patients with CHF after ST-segment elevation MI who are hospitalized for prolonged periods, nonambulatory, or are considered at high risk for DVT and are not receiving other anticoagulant therapy.¹⁴⁵

Also recommended by ACC and AHA for prophylaxis in patients surviving ST-segment elevation MI with or without acute ischemic stroke who have cardiac sources of embolism (atrial fibrillation, mural thrombus, akinetic segment) after reperfusion therapy; administer until adequate anticoagulation with warfarin achieved.¹⁴⁵

ACC and AHA suggest LMW heparin as reasonable alternative to unfractionated heparin in patients with ST-segment elevation MI who are not receiving thrombolytic therapy, provided no contraindications to anticoagulation exist.¹⁴⁵

Based on limited evidence principally with enoxaparin, ACC, AHA, and other clinicians suggest use of an LMW heparin as an alternative to unfractionated heparin in patients with acute ST-segment elevation MI undergoing PCI.⁹⁴

Dalteparin Sodium Dosage and Administration

General

• 
  

  Dosage adjustment and routine monitoring of coagulation parameters generally not necessary if recommended regimens are followed.^{1 152}

  
  


• 
  

  Monitoring LMW heparin therapy may be helpful in high-risk patient groups, such as pregnant women, patients with renal impairment, or patients at extremes of weight; use anti-factor Xa concentrations to monitor the anticoagulant effects of dalteparin.¹⁵²

  
  


• 
  

  In pregnant women with mechanical prosthetic heart valves, frequently monitor peak and trough anti-factor X_a concentrations; adjust dosage as necessary.^{111 153} ACCP and other clinicians recommend twice-daily dosing of LMW heparin in pregnant women, at least initially, because of the altered pharmacokinetics of these drugs (e.g., shorter half-life) in such women.^{117 153}

  
  

Administration

Sub-Q Administration

Administer by deep sub-Q injection; do not give IM.¹ Administer in sitting or supine position.¹ When injecting, insert entire length of needle at 45–90° angle.¹ Administer injections into the U-shaped area around the navel, upper outer aspect of the thigh, or upper outer quadrangle of the buttock.¹ Alternate injection sites daily.¹ When injecting into area around the navel or the thigh, insert needle into a skin fold created by thumb and forefinger.¹ Hold skin until needle is withdrawn.¹ Injection is commercially available in prefilled syringes equipped with a 27-gauge ½-inch needle.¹

Dosage

Dosages for dalteparin sodium and regular (unfractionated heparin) or other LMW heparins cannot be used interchangeably on a unit-for-unit (or mg-for-mg) basis.^{1 3 5 9}

Available as dalteparin sodium; dosage expressed in anti-Factor Xa international units (IU, units).^{1 2}

Adults

Unstable Angina and Non-ST-Segment Elevation/Non-Q-Wave MI

Sub-Q

120 units/kg every 12 hours (up to a maximum of 10,000 units every 12 hours) until patient is clinically stabilized, generally for 5–8 days.¹ Concurrent aspirin therapy is recommended in all patients unless contraindicated.¹

Prevention of Venous Thrombosis and Pulmonary Embolism

Hip-Replacement Surgery

Sub-Q

Initiate therapy either preoperatively or postoperatively; several regimens have been used.^{1 118} ACCP recommends initiation 12–24 hours postoperatively following achievement of hemostasis in patients at high risk for bleeding.¹¹⁸

Preoperative start, evening before surgery: 5000 units 10–14 hours before surgery, followed by 5000 units 4–8 hours after surgery or later if hemostasis has not been achieved.¹ Continue with 5000 units daily throughout the postoperative period (generally 5–10 days, but up to 14 days has been well tolerated).¹

Preoperative start, day of surgery: 2500 units within 2 hours prior to surgery, followed by 2500 units 4–8 hours after surgery or later if hemostasis has not been achieved.¹ Continue with 5000 units daily throughout the postoperative period (generally 5–10 days, but up to 14 days has been well tolerated).¹

Alternative preoperative regimen recommended by ACCP: usual high-risk dosage (e.g., 5000 units) beginning 12 hours prior to surgery and continuing for ≥10 days postoperatively.¹¹⁸

Postoperative start: 2500 units 4–8 hours after surgery or later if hemostasis has not been achieved.¹ Continue with 5000 units daily throughout the postoperative period (generally 5–10 days, but up to 14 days has been well tolerated).¹

Alternative postoperative regimen recommended by ACCP: half the usual high-risk dosage (e.g., 2500 units) 4–6 hours after surgery , followed by the usual high-risk dosage (e.g., 5000 units daily) the next day for ≥10 days.¹¹⁸

Another alternative regimen recommended by ACCP: Usual high-risk dosage (e.g., 5000 units) 12–24 hours after surgery and continuing for ≥10 days.¹¹⁸

Extended prophylaxis: ACCP recommends continuation for ≤28–35 days postoperatively in patients considered at high risk for thromboembolism.¹¹⁸

Hip-Fracture Surgery

Sub-Q

ACCP recommends the usual high-risk dosage (e.g., 5000 units daily) initiated either preoperatively or postoperatively.¹¹⁸ If surgery likely to be delayed, initiate preoperatively and reinstitute postoperatively after hemostasis achieved.¹¹⁸

Continue prophylaxis for ≥10 days (i.e., most patients will continue anticoagulation following hospital discharge).¹¹⁸

Extended prophylaxis: ACCP recommends continuation for ≤28–35 days postoperatively in patients considered at high risk for thromboembolism.¹¹⁸

Knee-Replacement Surgery

Sub-Q:

ACCP recommends the usual high-risk dosage (e.g., 5000 units daily) initiated either preoperatively or postoperatively.¹¹⁸

Continue prophylaxis for ≥10 days (i.e., most patients will continue anticoagulation following hospital discharge).¹¹⁸

General Surgery

Sub-Q

Patients at moderate to high risk for thromboembolic complications: 2500 units initially,^{1 5 6 7 8 9 27 30 90} given 1–2 hours before surgery.^{1 6 8 9 19 21 90} Continue with 2500 units once daily throughout postoperative period, generally for 5–10 days, until the risk of DVT has diminished.^{1 6 7 8 9 10 19 20 21 90 118}

Patients who are at high risk for thromboembolic complications: 5000 units on the evening prior to surgery (e.g., 8–12 hours prior to surgery).^{1 90} Such patients include those with malignant disease or a history of DVT or pulmonary embolism.^{1 90} Continue with 5000 units daily throughout the postoperative period, generally for 5–10 days.^{1 27 30 33}

Patients with malignancy: 2500 units given 1–2 hours prior to surgery and repeated 12 hours later.¹ Continue with 5000 units daily throughout the postoperative period, generally for 5–10 days.^{1 27 30 33}

Extended prophylaxis: ACCP suggests continuation for 2–3 weeks after hospital discharge in patients at high risk for thromboembolism (e.g., major cancer surgery).

Medical Conditions Associated with Thromboembolism

Sub-Q

5000 units once daily, generally for 12–14 days.¹ Alternatively, ACCP recommends a dosage of 2500 units daily in general medical patients with high-risk factors for thromboembolism (e.g., cancer, CHF, severe lung disease, patients confined to bedrest).⁹⁰

Thromboembolism Occurring During Pregnancy

Sub-Q

Treatment of acute venous thromboembolism: 200 units/kg daily in 1 or 2 divided doses throughout pregnancy.¹¹⁷ Continue oral anticoagulation (e.g., with warfarin) for at least 6 weeks postpartum.¹¹⁷

Primary prevention in women with inherited causes of thrombophilia (e.g., antithrombin deficiency, heterozygous genetic mutation of both prothrombin G20210A and factor V Leiden, or homozygous genetic mutation for factor V Leiden or prothrombin G20210A): 5000 units once daily or every 12 hours throughout pregnancy suggested, followed by postpartum oral anticoagulation (e.g., with warfarin) for at least 4–6 weeks.¹¹⁷

Primary prevention in other patients with confirmed thrombophilia: 5000 units once daily throughout pregnancy suggested, followed by postpartum oral anticoagulation (e.g., with warfarin) for at least 4–6 weeks.¹¹⁷

Secondary prevention after a single episode of idiopathic venous thromboembolism in women not receiving long-term anticoagulation: 5000 units once daily throughout pregnancy suggested, followed by postpartum oral anticoagulation (e.g., with warfarin) for at least 4–6 weeks.¹¹⁷

Secondary prevention after a single episode of venous thromboembolism in women with risk factors (e.g., confirmed thrombophilia, strong family history of thrombosis) not receiving long-term anticoagulation: 5000 units once daily or every 12 hours throughout pregnancy suggested, followed by postpartum oral anticoagulation (e.g., with warfarin) for at least 4–6 weeks.¹¹⁷

Secondary prevention after >2 episodes of venous thromboembolism in women receiving long-term anticoagulation: 200 units/kg daily in 1 or 2 divided doses throughout pregnancy suggested, followed by postpartum resumption of long-term anticoagulation.¹¹⁷

Adjust dosage for extremes of body weight.¹¹⁷

Discontinue 24 hours prior to elective induction of labor.¹¹⁷

Embolism Associated with Atrial Fibrillation/Flutter

Sub-Q

Patients with atrial fibrillation duration <48 hours undergoing cardioversion who have no contraindications to anticoagulation: 200 units/kg daily in 1 or 2 divided doses.^{116 117 126 127}

ACCP suggests same regimen for anticoagulation in patients undergoing cardioversion for atrial flutter.¹¹⁹

Treatment of DVT and Nonmassive Pulmonary Embolism

Sub-Q

200 units/kg daily in 1 or 2 divided doses for at least 5 days has been recommended; administer on outpatient basis in selected patients with acute uncomplicated DVT.¹¹⁶

ACCP recommends against routine monitoring of anticoagulation (e.g., anti-factor X_a activity) with heparin treatment of acute venous thromboembolism.¹¹⁶

Initiate concurrently with oral anticoagulation (e.g., with warfarin) and overlap therapy until response to warfarin is adequate.¹¹⁶ Continue oral anticoagulation for at least 3 months.^{117 126 127}

Patients with cancer or in whom oral anticoagulation contraindicated or inconvenient:^{39 59 116} 200 units/kg once daily for 1 month, followed by 150 units/kg once daily for at least 3–6 months.¹¹⁶ Continue anticoagulation indefinitely or until cancer is resolved.¹¹⁶

Prescribing Limits

Adults

Unstable Angina or Non-ST-Segment Elevation/Non-Q-Wave MI

Sub-Q

Maximum 10,000 units every 12 hours.¹

Cautions for Dalteparin Sodium

Contraindications

• 
  

  Known hypersensitivity to dalteparin, heparin, or pork products.¹

  
  


• 
  

  Active major bleeding or thrombocytopenia associated with positive in vitro tests for anti-platelet antibody in the presence of the drug.¹

  
  


• 
  

  Patients with unstable angina or non-ST-segment elevation/non-Q-wave MI undergoing regional anesthesia.¹

  
  

Warnings/Precautions

Warnings

Neurologic Effects

Epidural or spinal hematomas and neurologic injury, including long-term or permanent paralysis, associated with concurrent use of low molecular weight (LMW) heparins and neuraxial (spinal/epidural) anesthesia or spinal puncture procedures.^{1 35 77} Frequent monitoring for signs of neurologic impairment recommended.³⁵ (See Boxed Warning.)

Hematologic Effects

As with other anticoagulants, bleeding may occur at any site during therapy.¹ Use with extreme caution in patients with an increased risk of hemorrhage.¹ Such patients include those with severe uncontrolled hypertension, bacterial endocarditis, congenital or acquired bleeding disorders, active ulceration and angiodysplastic GI disease, hemorrhagic stroke, or recent brain, spinal, or ophthalmologic surgery.¹ Use with caution in patients with bleeding diathesis or recent GI bleeding.¹

An unexpected decrease in hematocrit or BP may indicate hemorrhage and should prompt evaluation to determine a bleeding site.¹ If severe hemorrhage or dalteparin overdosage occurs, administer protamine sulfate immediately.¹

If a thromboembolic event occurs despite dalteparin prophylaxis, the drug should be discontinued and appropriate therapy initiated.¹

Thrombocytopenia with thrombosis reported rarely.¹ Heparin-induced thrombocytopenia can occur.¹

Use with extreme caution in patients with a history of heparin-induced thrombocytopenia.¹ Use with caution in patients with thrombocytopenia or platelet defects.¹

Monitor thrombocytopenia of any degree closely.¹

Sensitivity Reactions

Allergic reactions^{1 19 33 34} (including pruritus,^{1 6 11} rash,¹ fever,¹ injection site reactions,^{1 6 11 12} and bullous eruptions)¹ and skin necrosis^{1 34} have occurred rarely.¹ Anaphylactoid reactions¹ also reported.¹

General Precautions

Hepatic Effects

Increases in serum aminotransferase concentrations reported.^{1 21 34}

Because serum aminotransferase determinations are important in the differential diagnosis of MI, liver disease, and pulmonary emboli, interpret elevation of these enzymes during therapy with caution.¹

Specific Populations

Pregnancy

Category B.¹ Because benzyl alcohol may cross the placenta, dalteparin in multiple-dose vials containing benzyl alcohol should not be used in pregnant women.⁶⁷

Lactation

Small amounts distributed into breast milk.^{5 36} Use with caution in nursing women.¹

Pediatric Use

Safety and efficacy not established.^{1 30}

Multiple-dose vials contain benzyl alcohol as a preservative.¹ Administration of injections preserved with benzyl alcohol has been associated with toxicity in neonates.^{1 67 68 69 70 71 72} However, the presence of small amounts of benzyl alcohol in a commercially available injection should not proscribe its use in neonates.

Geriatric Use

Because geriatric patients may have decreased renal function and because patients with severe renal impairment may be at increased risk of dalteparin-induced toxicity.¹ Pay careful attention to dosing intervals and concomitant agents (particularly antiplatelet agents), particularly in geriatric patients with low body weight (<45 kg) and those predisposed to decreased renal function.¹

Hepatic Impairment

Use with caution in patients with severe hepatic impairment.¹

Renal Impairment

Use with caution in patients with severe renal impairment or hypertensive or diabetic nephropathy.¹

Common Adverse Effects

Hematoma at the injection site.^{1 8 9 10 19 20 21 33 34}

Interactions for Dalteparin Sodium

Specific Drugs

Drug	Interaction	Comments
Oral anticoagulants	Increased risk of bleeding1	Use concomitantly with care1
Platelet-aggregation inhibitors	Increased risk of bleeding1	Use concomitantly with care1
Thrombolytic agents	Increased risk of bleeding1	Use concomitantly with care1

Dalteparin Sodium Pharmacokinetics

Absorption

Bioavailability

Approximately 87% (absolute bioavailability).¹ Greater bioavailability than unfractionated heparin (based on anti-factor Xa activity).^{1 3 5 6 7 8 27 29}

Distribution

Extent

40–60 mL/kg (based on anti-Factor Xa activity).¹

Not known if distributed into milk.¹

Elimination

Half-life

3–5 hours (sub-Q administration).¹

Special Populations

Terminal half-life prolonged (to 5.7 hours) in patients with chronic renal insufficiency requiring hemodialysis compared with healthy individuals.¹

Similar pharmacokinetics in geriatric and younger patients.⁵

Stability

Storage

Parenteral

Solution for Injection

20–25°C.¹

Compatibility

For information on systemic interactions resulting from concomitant use, see Interactions.

Should not be mixed with other injections or infusions unless specific compatibility data support such admixtures.¹

ActionsActions

• 
  

  Less effect on thrombin than unfractionated heparin at a given level of anti-factor Xa activity.^{1 3 27}

  
  


• 
  

  At recommended dosages, does not substantially affect platelet aggregation, fibrinolysis, global clotting function tests (i.e., PT, thrombin time, aPTT), or lipoprotein lipase.^{1 8 24 25 31}

  
  

Advice to Patients

• 
  

  Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.¹

  
  


• 
  

  Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs.¹

  
  


• 
  

  Importance of informing patients of other important precautionary information.¹ (See Cautions.)

  
  

Preparations

Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.

Dalteparin Sodium (Porcine)

Routes	Dosage Forms	Strengths	Brand Names	Manufacturer
Parenteral	Injection, for subcutaneous use only	2500 units/0.2 mL	Fragmin (preservative-free; available as 0.2-mL disposable syringe)	Eisai
		5000 units/0.2 mL	Fragmin (preservative-free; available as 0.2-mL disposable syringe)	Eisai
		7500 units/0.3 mL	Fragmin (preservative-free; available as 0.3 mL disposable syringe)	Eisai
		10,000 units/ mL	Fragmin (preservative-free; available as 1 mL disposable syringe and with benzyl alcohol 14 mg/mL available in 9.5 mL multiple-dose vial)	Eisai
		25,000 units/mL	Fragmin (with benzyl alcohol 14 mg/mL available 3.8 mL multiple-dose vial)	Eisai

Disclaimer

This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.

The American Society of Health-System Pharmacists, Inc. and Drugs.com re

Piludog

Piludog may be available in the countries listed below.

In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for Piludog

Megestrol

Megestrol 17α-acetate (a derivative of Megestrol) is reported as an ingredient of Piludog in the following countries:

• Portugal

International Drug Name Search

Gentamicin Actavis

Gentamicin Actavis may be available in the countries listed below.

Ingredient matches for Gentamicin Actavis

Gentamicin

Gentamicin sulfate (a derivative of Gentamicin) is reported as an ingredient of Gentamicin Actavis in the following countries:

• Bulgaria

International Drug Name Search

Finigas

Finigas may be available in the countries listed below.

Ingredient matches for Finigas

Dimeticone

Dimeticone is reported as an ingredient of Finigas in the following countries:

• Brazil

International Drug Name Search

Detrichol

Detrichol may be available in the countries listed below.

Ingredient matches for Detrichol

Gemfibrozil

Gemfibrozil is reported as an ingredient of Detrichol in the following countries:

• Indonesia

International Drug Name Search

Adco-Paracetamol

Adco-Paracetamol may be available in the countries listed below.

Ingredient matches for Adco-Paracetamol

Paracetamol

Paracetamol is reported as an ingredient of Adco-Paracetamol in the following countries:

• South Africa

International Drug Name Search

Dytac

Dytac may be available in the countries listed below.

UK matches:

• Dytac 50mg Capsules (SPC)

Ingredient matches for Dytac

Triamterene

Triamterene is reported as an ingredient of Dytac in the following countries:

• Belgium


• United Kingdom

International Drug Name Search

Glossary

SPC	Summary of Product Characteristics (UK)

Click for further information on drug naming conventions and International Nonproprietary Names.

Intercon

Intercon may be available in the countries listed below.

Ingredient matches for Intercon

Mometasone

Mometasone 17-(2-furoate) (a derivative of Mometasone) is reported as an ingredient of Intercon in the following countries:

• Indonesia

International Drug Name Search

Glaufos

Glaufos may be available in the countries listed below.

Ingredient matches for Glaufos

Ofloxacin

Ofloxacin is reported as an ingredient of Glaufos in the following countries:

• Georgia

International Drug Name Search

Sodium Bicarbonate

In some countries, this medicine may only be approved for veterinary use.

In the US, Sodium Bicarbonate (sodium bicarbonate systemic) is a member of the following drug classes: antacids, minerals and electrolytes, urinary pH modifiers and is used to treat Asystole, Diabetic Ketoacidosis, Hyperkalemia, Hyperuricemia Secondary to Chemotherapy, Indigestion, Metabolic Acidosis and Urinary Alkalinization.

US matches:

• Sodium Bicarbonate


• Sodium Bicarbonate Tablets


• Sodium Bicarbonate/Citric Acid/Simethicone Effervescent Granule Packets


• Sodium bicarbonate Oral, Intravenous, Subcutaneous

UK matches:

• Sodium Bicarbonate (Boots Company plc)
• Sodium Bicarbonate BP (Boots Company plc) (SPC)
• Sodium Bicarbonate Injection Bp Minijet 8.4% (International Medication Systems) (SPC)
• Sodium Bicarbonate Injection Minijet 4.2% (International Medication Systems) (SPC)

Scheme

USP

ATC (Anatomical Therapeutic Chemical Classification)

B05CB04,B05XA02

CAS registry number (Chemical Abstracts Service)

0000144-55-8

Chemical Formula

Na-H-C-O3

Molecular Weight

84

Therapeutic Category

Alkalinizer

Chemical Name

Carbonic acid monosodium salt

Foreign Names

• Natrii hydrogeni carbonas (Latin)
• Natriumhydrogencarbonat (German)
• Bicarbonate de sodium (French)
• Sodio bicarbonato (Spanish)

Generic Names

• Sodium (bicarbonate de) (OS: DCF)
• Sodium Bicarbonate (OS: JAN)
• E 500 (IS)
• Monosodium carbonate (IS)
• Natriumbikarbonat (IS)
• Natron (IS)
• Natron, doppeltkohlensaures (IS)
• Bicarbonate de sodium (PH: Ph. Eur. 6)
• Natiumhydrogencarbonat (PH: Ph. Eur. 6)
• Natrii hydrogeni carbonas (PH: Ph. Eur. 5)
• Natrii hydrogenocarbonas (PH: Ph. Int. 4, Ph. Eur. 6)
• Sodium Bicarbonate (PH: BP 2010, JP XIV, USP 32)
• Sodium Hydrogen Carbonate (PH: Ph. Int. 4, Ph. Eur. 6)

Brand Names

• Acidosan (veterinary use)
  Vetoquinol, Switzerland



• Alginate de sodium/Bicarbonate de sodium Biogaran (Sodium Bicarbonate and Sodium Alginate)
  Biogaran, France



• Alginate de sodium/Bicarbonate de sodium EG (Sodium Bicarbonate and Sodium Alginate)
  EG Labo, France



• Alginate de sodium/Bicarbonate de sodium Sandoz (Sodium Bicarbonate and Sodium Alginate)
  Sandoz, France



• Alginate de sodium/Bicarbonate de sodium Teva (Sodium Bicarbonate and Sodium Alginate)
  Teva Santé, France



• Alkala
  Sanum-Kehlbeck, Germany



• Alkaligen
  Teva, Hungary



• Alka-Selzer (Sodium Bicarbonate and Acetylsalicylic Acid)
  Bayer, Canada



• Arm & Hammer
  Church & Dwight, United States



• Aromag (Sodium Bicarbonate and Magnesium Carbonate light)
  ICM, Singapore



• AZ (Sodium Bicarbonate and Sodium Gualenate)
  Nipro PharmaNipurofama, Japan



• Babic
  Teva, Israel



• Balgin
  Kyosei Seiyaku, Japan



• Baros
  Horii Yakuhin, Japan



• Barytgen
  Fushimi Seiyaku, Japan



• Berin
  Taiyo Pharmaceutical, Japan



• Bibag
  Fresenius Medical Care, France



• BicaNorm
  Fresenius, Germany; Fresenius Medical Care, Ireland



• Bicarbonaat (veterinary use)
  Eurovet, Netherlands



• Bicarbonat de Sodiu
  Braun, Romania



• Bicarbonate de Sodium B. Braun
  Braun, France



• Bicarbonate de Sodium Baxter
  Baxter, France; Baxter, Luxembourg



• Bicarbonate de Sodium Biosedra
  Fresenius, France



• Bicarbonate de Sodium Cooper
  Cooper, France



• Bicarbonate de Sodium Lavoisier
  Chaix et du Marais, France



• Bicarbonate de Sodium Renaudin
  Renaudin, France



• Bicarbonate Monosodique
  Siphat, Tunisia



• Bicarbonato de Sodio Ecar
  Ecar, Colombia



• Bicarbonato de Sodio EWE
  Sanitas, Argentina



• Bicarbonato de Sódio Labesfal
  Labesfal, Portugal



• Bicarbonato de Sodio Püler
  H. Medica, Argentina



• Bicarbonato de Sodio
  Behrens, Venezuela; Biosano, Chile; Farmionni, Colombia; Fecofar, Argentina; Oriental, Argentina; Qualicont, Peru; Reccius, Chile; Sanderson, Chile; UQP, Peru



• Bicarbonato de Sosa T M
  Novartis, Spain



• Bicarbonato Sod Agadrian
  Tecnisan, Spain



• Bicarbonato Sod Bieffe M
  Baxter, Spain



• Bicarbonato Sod Cinfa
  Cinfa, Spain



• Bicarbonato Sod Grifols
  Grifols, Spain



• Bicarbonato Sod Orravan
  Orravan, Spain



• Bicarbonato Sod Pege
  Puerto Galiano, Spain



• Bicarbonato Sod Serra
  Serra Pamies, Spain



• Bicarbonato Sod Viviar
  Viviar, Spain



• Bicarbonato Sodico Braun
  Braun, Spain



• Bicarbonato Sodico Mein
  Fresenius, Spain



• Bicardial B
  Trifarma, Peru



• Bicarsodio
  Trifarma, Peru



• Bullrich Salz
  Delta Pronatura, Austria



• Citrocarbonate
  Lee, United States



• Compudose (Sodium Bicarbonate and Estradiol (veterinary use))
  Elanco Animal Health, South Africa



• Concentre Basique BC-F
  Fresenius-Tunisie, Tunisia



• Corega
  GlaxoSmithKline, Argentina



• Darbie
  General Drugs House, Thailand



• Eductyl (Sodium Bicarbonate and Potassium Hydrogen Tartrate)
  Techni-Pharma, Monaco



• Eductyl enfant (Sodium Bicarbonate and Potassium Hydrogen Tartrate (pediatric))
  Techni-Pharma, Monaco



• Effersol (Sodium Bicarbonate and Calcium Citrate)
  Aspen Pharmacare Consumer, South Africa



• Electrolade
  Eastern, Ireland



• Enhos
  Kansuk, Turkey



• Gastrast K
  Toho Kagaku, Japan



• Gastrast T
  Toho Kagaku, Japan



• Gaviscon (Sodium Bicarbonate and Alginic Acid)
  Pekit, Greece; Reckitt Benckiser, Belgium; Reckitt Benckiser, South Africa; Reckitt Benckiser-UK, Italy



• Gaviscon (Sodium Bicarbonate and Sodium Alginate, + Calcium Carbonate)
  Reckitt Benckiser, Thailand



• Gaviscon (Sodium Bicarbonate and Sodium Alginate)
  Reckitt Benckiser, France



• Gaviscon Nourrisson (Sodium Bicarbonate and Sodium Alginate (pediatric))
  Reckitt Benckiser, France



• Gavisconell (Sodium Bicarbonate and Sodium Alginate)
  Reckitt Benckiser, France



• Hachiazule (Sodium Bicarbonate and Sodium Gualenate)
  Toyo Seiyaku KaseiOriental, Japan



• Hospasol
  Hospal, Spain



• Incarbon (Sodium Bicarbonate and Sodium Phosphate)
  Taiyo Pharmaceutical, Japan



• Jutamin
  Fuso Pharmaceutical, Japan



• Koncentrovani
  Zorka, Serbia



• Lecicarbon (Sodium Bicarbonate and Potassium tartrate)
  Brady, Austria



• Lecicarbon (Sodium Bicarbonate and Sodium Phosphate)
  Athenstaedt, Switzerland; Athenstaedt, Germany



• Lecicarbon (Sodium Bicarbonate and Sodium Phosphate (pediatric))
  Athenstaedt, Switzerland



• Magnesie Plus (Sodium Bicarbonate and Calcium Carbonate, + Magnesium Carbonate)
  Omega, Belgium



• Meylon
  Otsuka, Japan



• Molar Sodyum Bicarbonat
  Drogsan, Turkey; Galen, Turkey; Osel, Turkey



• Nanakid
  PD Chemical, Myanmar



• Natrijev hidrogenkarbonat
  Medis, Slovenia



• Natrij-hidrogenkarbonat Pliva
  Pliva, Croatia (Hrvatska)



• Natrij-hidrogenkarbonat
  HZTM, Croatia (Hrvatska)



• Natrium bicarbonat ACS Dobfar Info
  ACS Dobfar Info, Switzerland



• Natrium bicarbonat B.Braun
  B. Braun Medical, Switzerland



• Natrium Bicarbonicum Bichsel
  Bichsel, Switzerland



• Natrium Bicarbonicum Sintetica
  Sintetica, Switzerland



• Natrium bicarbonicum
  Polpharma, Poland



• Natrium-Bicarbonat B.Braun
  B. Braun Medical, Switzerland



• Natriumbicarbonat Fresenius
  Fresenius, Serbia; Fresenius Kabi, Austria



• Natriumbicarbonat SAD
  Amgros, Denmark



• Natriumbicarbonate Braun
  Braun, Finland



• Natriumbikarbonat Fresenius Kabi
  Fresenius, Sweden



• Natriumbikarbonat isotonisk SAD
  Amgros, Denmark



• Natriumbikarbonat Recip
  Recip, Sweden



• Natriumbikarbonat
  Recip, Iceland



• Natriumhydrogencarbonat B.Braun
  B.Braun, Germany



• Natriumhydrogencarbonat Fresenius
  Fresenius, Bosnia & Herzegowina; Fresenius, Luxembourg



• Natriumhydrogencarbonat Infusionslösung
  Fresenius, Germany



• Natriumhydrogencarbonat-Braun
  Braun Melsungen, Luxembourg



• Natriumhydrogencarbonat-Lösung Baxter
  Baxter, Germany



• Natriumhydrogencarbonat-Lösung DeltaSelect
  DeltaSelect, Germany



• Natriumhydrogencarbonat-Lösung Köhler
  Köhler, Germany



• Nephrotrans
  Medice, Germany; Salmon, Switzerland



• Neut
  Hospira, United States



• New Lecicarbon (Sodium Bicarbonate and Sodium Phosphate)
  Kyoto Yakuhin, Japan



• Prebinate
  Uji Seiyaku, Japan



• Soda Mint
  CMC, United States



• Sodibic
  Aspen, Australia



• Sodio Bicarbonato
  Bieffe, Italy; Bioindustria Lim, Italy; Diaco, Italy; Eurospital, Italy; Farmacologico, Italy; Fresenius, Italy; Galenica, Italy; Monico, Italy; Nova Argentia, Italy; NovaSelect, Italy; Ogna, Italy; Salf, Italy; Sella, Italy; Zeta, Italy



• Sodio Bicarbonato (veterinary use)
  Galenica Senese, Italy; NovaSelect vet, Italy; Panpharma vet, Italy



• Sodium Bicarbonate Biomed
  Biomed, New Zealand



• Sodium Bicarbonate Braun
  Braun, Estonia; Braun, Lithuania



• Sodium Bicarbonate Pfrimmer
  Kalbe, Indonesia



• Sodium Bicarbonate
  ABM, New Zealand; AFT, New Zealand; APP, United States; Baxter, United States; Braun, Latvia; Chi Sheng, Taiwan; CMC, United States; CSL, Australia; CSL Biotherapies, New Zealand; David Craig, New Zealand; Fresenius, Malta; Hospira, Canada; Hospira, United States; IMS, Oman; International Medication Systems, United Kingdom; LCM, Malta; Phebra, Australia; Rugby, United States; United Research, United States; PfizerPerth, Australia



• Solucion Bicarbonato de Sodio
  Sanderson, Chile



• Soluciones Parenterales
  Fidex, Argentina



• Solurrinol (Sodium Bicarbonate and Potassium Chloride)
  Teofarma, Spain



• Soluzione di Sodio Bicarbonato (veterinary use)
  Izo, Italy



• Tansonin
  Mylan Pharmaceutical, Japan



• Venofusin Bicarb Sodico
  Fresenius, Spain

International Drug Name Search

Glossary

DCF	Dénomination Commune Française
IS	Inofficial Synonym
JAN	Japanese Accepted Name
OS	Official Synonym
PH	Pharmacopoeia Name
SPC	Summary of Product Characteristics (UK)
USP	Pharmacopoeia of the United States

Click for further information on drug naming conventions and International Nonproprietary Names.

Syrup Zinc Asiatic Lab

Syrup Zinc Asiatic Lab may be available in the countries listed below.

Ingredient matches for Syrup Zinc Asiatic Lab

Zinc Sulfate

Zinc Sulfate is reported as an ingredient of Syrup Zinc Asiatic Lab in the following countries:

• Bangladesh

International Drug Name Search

TriLipix

In the US, TriLipix (fenofibric acid systemic) is a member of the drug class fibric acid derivatives and is used to treat High Cholesterol and Hypertriglyceridemia.

US matches:

• Trilipix


• Trilipix Delayed-Release Capsules

Ingredient matches for TriLipix

Fenofibrate

Fenofibrate is reported as an ingredient of TriLipix in the following countries:

• United States

International Drug Name Search

Scansepta Solution

Scansepta Solution may be available in the countries listed below.

Ingredient matches for Scansepta Solution

Povidone Iodine

Povidone-Iodine is reported as an ingredient of Scansepta Solution in the following countries:

• Indonesia

International Drug Name Search

Cervep

Cervep may be available in the countries listed below.

Ingredient matches for Cervep

Heparin

Heparin sodium salt (a derivative of Heparin) is reported as an ingredient of Cervep in the following countries:

• Argentina

International Drug Name Search

Mepron

Mepron is a brand name of atovaquone, approved by the FDA in the following formulation(s):

MEPRON (atovaquone - suspension; oral)

• 
  Manufacturer: GLAXOSMITHKLINE LLC
  
  Approval date: February 8, 1995
  
  Strength(s): 750MG/5ML ^[RLD]

Has a generic version of Mepron been approved?

No. There is currently no therapeutically equivalent version of Mepron available.

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Mepron. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.

Related Patents

Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.

• 
  Atovaquone pharmaceutical compositions
  Patent 6,649,659
  Issued: November 18, 2003
  Inventor(s): Alan Roy; Dearn
  Assignee(s): SmithKline Beecham Corporation
  The invention relates to a process for the production of microfluidized particles of atovaquone having improved bioavailability.
  
  Patent expiration dates:
  
  
  • July 10, 2016
    
    ✓ 
    Patent use: TREATMENT OF PNEUMOCYSTIS CARINII INFECTIONS
    ✓ 
    Drug substance
    ✓ 
    Drug product
  
  
  
  • January 10, 2017
    
    ✓ 
    Pediatric exclusivity
  
  

See also...

• Mepron Consumer Information (Wolters Kluwer)
• Mepron Consumer Information (Cerner Multum)
• Mepron Advanced Consumer Information (Micromedex)
• Mepron AHFS DI Monographs (ASHP)
• Atovaquone Consumer Information (Wolters Kluwer)
• Atovaquone Consumer Information (Cerner Multum)
• Atovaquone Advanced Consumer Information (Micromedex)
• Atovaquone AHFS DI Monographs (ASHP)

Ventar

Ventar may be available in the countries listed below.

Ingredient matches for Ventar

Salbutamol

Salbutamol sulfate (a derivative of Salbutamol) is reported as an ingredient of Ventar in the following countries:

• Philippines

International Drug Name Search

Encephabol

Encephabol may be available in the countries listed below.

Ingredient matches for Encephabol

Pyritinol

Pyritinol is reported as an ingredient of Encephabol in the following countries:

• Austria


• Luxembourg


• Mexico

Pyritinol dihydrochloride (a derivative of Pyritinol) is reported as an ingredient of Encephabol in the following countries:

• Austria


• Bahrain


• Cyprus


• Czech Republic


• Egypt


• Georgia


• Germany


• Hong Kong


• India


• Indonesia


• Iran


• Iraq


• Jordan


• Kuwait


• Latvia


• Lebanon


• Luxembourg


• Mexico


• Oman


• Philippines


• Qatar


• Romania


• Russian Federation


• Saudi Arabia


• South Africa


• Sudan


• Thailand


• United Arab Emirates


• Yemen

International Drug Name Search

Colchidrint

Colchidrint may be available in the countries listed below.

Ingredient matches for Colchidrint

Colchicine

Colchicine is reported as an ingredient of Colchidrint in the following countries:

• Peru

International Drug Name Search

Pharmatex

Pharmatex may be available in the countries listed below.

Ingredient matches for Pharmatex

Benzalkonium Chloride

Benzalkonium chloride (a derivative of Benzalkonium) is reported as an ingredient of Pharmatex in the following countries:

• Algeria


• Argentina


• Estonia


• France


• Georgia


• Hungary


• Israel


• Latvia


• Lithuania


• Luxembourg


• Portugal


• Romania


• Russian Federation


• Serbia


• Slovakia


• Tunisia

International Drug Name Search

Modiem

Modiem may be available in the countries listed below.

Ingredient matches for Modiem

Cefonicid

Cefonicid disodium salt (a derivative of Cefonicid) is reported as an ingredient of Modiem in the following countries:

• Italy

International Drug Name Search

Piridostigmina bromuro

Piridostigmina bromuro may be available in the countries listed below.

Ingredient matches for Piridostigmina bromuro

Pyridostigmine

Piridostigmina bromuro (DCIT) is known as Pyridostigmine in the US.

International Drug Name Search

Glossary

DCIT	Denominazione Comune Italiana

Click for further information on drug naming conventions and International Nonproprietary Names.

Bucladesine

Scheme

Rec.INN

ATC (Anatomical Therapeutic Chemical Classification)

C01CE04

CAS registry number (Chemical Abstracts Service)

0000362-74-3

Chemical Formula

C18-H24-N5-O8-P

Molecular Weight

469

Therapeutic Category

Cardiac stimulant, cardiotonic agent

Chemical Name

N-(9-ß-D-Ribofuranosyl-9H-purin-6-yl)butyramide cyclic 3',5'-(hydrogen phosphate)-2'-butyrate

Foreign Names

• Bucladesinum (Latin)
• Bucladesin (German)
• Bucladesine (French)
• Bucladesina (Spanish)

Brand Names

• Actosin
  Daiichi Sankyo, Japan; Nipro GenephaNipurojenefa, Japan

International Drug Name Search

Glossary

Rec.INN

Recommended International Nonproprietary Name (World Health Organization)

Click for further information on drug naming conventions and International Nonproprietary Names.

Mometasone Help

Mometasone Help may be available in the countries listed below.

Ingredient matches for Mometasone Help

Mometasone

Mometasone 17-(2-furoate) (a derivative of Mometasone) is reported as an ingredient of Mometasone Help in the following countries:

• Greece

International Drug Name Search

Citicolin

Citicolin may be available in the countries listed below.

Ingredient matches for Citicolin

Citicoline

Citicoline is reported as an ingredient of Citicolin in the following countries:

• Taiwan

Citicoline sodium salt (a derivative of Citicoline) is reported as an ingredient of Citicolin in the following countries:

• Italy

International Drug Name Search

Diclofénac Teva Conseil

Diclofénac Teva Conseil may be available in the countries listed below.

Ingredient matches for Diclofénac Teva Conseil

Diclofenac

Diclofenac diethylamine (a derivative of Diclofenac) is reported as an ingredient of Diclofénac Teva Conseil in the following countries:

• France

International Drug Name Search

L-Cysteine Domesco

L-Cysteine Domesco may be available in the countries listed below.

Ingredient matches for L-Cysteine Domesco

Cysteine

Cysteine is reported as an ingredient of L-Cysteine Domesco in the following countries:

• Vietnam

International Drug Name Search

Alvo

Alvo may be available in the countries listed below.

Ingredient matches for Alvo

Oxaprozin

Oxaprozin is reported as an ingredient of Alvo in the following countries:

• Japan

International Drug Name Search

Kinevac

Kinevac is a brand name of sincalide, approved by the FDA in the following formulation(s):

KINEVAC (sincalide - injectable; injection)

• 
  Manufacturer: BRACCO
  
  Approved Prior to Jan 1, 1982
  
  Strength(s): 0.005MG/VIAL ^[RLD]

Has a generic version of Kinevac been approved?

No. There is currently no therapeutically equivalent version of Kinevac available.

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Kinevac. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.

Related Patents

Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.

• 
  Sincalide formulations
  Patent 6,803,046
  Issued: October 12, 2004
  Inventor(s): Edmund C.; Metcalfe & Jo Anna; Monteferrante & Margaret; Newborn & Irene; Ropiak & Ernst; Schramm & Gregory W.; White & Julius P.; Zodda
  Assignee(s): Bracco International B.V.
  The invention features sincalide formulations that include an effective amount of sincalide, a bulking agent/tonicity adjuster, a stabilizer, a surfactant, a chelator, and a buffer. The invention also features kits and methods for preparing improved sincalide formulations, as well as methods for treating, preventing, and diagnosing gall bladder-related disorders using sincalide formulations.
  
  Patent expiration dates:
  
  
  • August 16, 2022
    
    ✓ 
    Drug product
  
  

See also...

• Kinevac Consumer Information (Cerner Multum)
• Kinevac Advanced Consumer Information (Micromedex)
• Sincalide Consumer Information (Cerner Multum)
• Sincalide Intravenous Advanced Consumer Information (Micromedex)

Ran-Lansoprazole

Ran-Lansoprazole may be available in the countries listed below.

Ingredient matches for Ran-Lansoprazole

Lansoprazole

Lansoprazole is reported as an ingredient of Ran-Lansoprazole in the following countries:

• South Africa

International Drug Name Search

Promethazine PCH

Promethazine PCH may be available in the countries listed below.

Ingredient matches for Promethazine PCH

Promethazine

Promethazine hydrochloride (a derivative of Promethazine) is reported as an ingredient of Promethazine PCH in the following countries:

• Netherlands

International Drug Name Search

Sulfafenazolo

Sulfafenazolo may be available in the countries listed below.

Ingredient matches for Sulfafenazolo

Sulfaphenazole

Sulfafenazolo (DCIT) is also known as Sulfaphenazole (Rec.INN)

International Drug Name Search

Glossary

DCIT	Denominazione Comune Italiana
Rec.INN	Recommended International Nonproprietary Name (World Health Organization)

Click for further information on drug naming conventions and International Nonproprietary Names.

Oxazepam-1A Pharma

Oxazepam-1A Pharma may be available in the countries listed below.

Ingredient matches for Oxazepam-1A Pharma

Oxazepam

Oxazepam is reported as an ingredient of Oxazepam-1A Pharma in the following countries:

• Germany

International Drug Name Search

Acido Salicilico Sella

Acido Salicilico Sella may be available in the countries listed below.

Ingredient matches for Acido Salicilico Sella

Salicylic Acid

Salicylic Acid is reported as an ingredient of Acido Salicilico Sella in the following countries:

• Italy

International Drug Name Search

Sonapax

Sonapax may be available in the countries listed below.

Ingredient matches for Sonapax

Thioridazine

Thioridazine is reported as an ingredient of Sonapax in the following countries:

• Georgia


• Russian Federation

International Drug Name Search

Mestil-Ka

Mestil-Ka may be available in the countries listed below.

Ingredient matches for Mestil-Ka

Menadione

Menadione sodium sulfonate (a derivative of Menadione) is reported as an ingredient of Mestil-Ka in the following countries:

• Argentina

International Drug Name Search

Chevicol plus

Chevicol plus may be available in the countries listed below.

In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for Chevicol plus

Dimetridazole

Dimetridazole is reported as an ingredient of Chevicol plus in the following countries:

• Austria

Paromomycin

Paromomycin sulfate (a derivative of Paromomycin) is reported as an ingredient of Chevicol plus in the following countries:

• Austria

International Drug Name Search

Omeprazole Sodium

Omeprazole Sodium may be available in the countries listed below.

Ingredient matches for Omeprazole Sodium

Omeprazole

Omeprazole Sodium (BANM, USAN) is known as Omeprazole in the US.

International Drug Name Search

Glossary

BANM	British Approved Name (Modified)
USAN	United States Adopted Name

Click for further information on drug naming conventions and International Nonproprietary Names.