Wandara IM/IV Injection 1 gm/vial Introduction

Wandara IM/IV Injection 1 gm/vial is an antibiotic belonging to the carbapenem class of antibiotics. It is commonly used to treat a wide range of bacterial infections. It is used to treat a variety of infections caused by susceptible gram-positive and gram-negative bacteria. It is also used to prevent infection in those undergoing certain surgical procedures. Wandara IM/IV Injection 1 gm/vial has excellent in vitro activity against Gram-positive and Gram-negative organisms, although there is some variation of activity depending on the isolate.

Uses for Wandara IM/IV Injection 1 gm/vial

Wandara IM/IV Injection 1 gm/vial is approved for use for infections of the abdomen, such as intra-abdominal abscesses and surgical infections; infections of the skin and upper respiratory tract; gynecologic infections, such as lower endometritis and pelvic help infections; intra-abdominal infections, such as cholangitis, cholecystitis, appendicitis; and urinary tract and prostate infections, such as pyelonephritis.

Brand Name Wandara
Type IM/IV Injection
Weight 1 gm/vial
Generic Ertapenem
Manufacturer Incepta Pharmaceuticals Ltd.
Available in English বাংলা

Mechanism of Action

Wandara IM/IV Injection 1 gm/vial inhibits bacterial cell wall synthesis by binding to penicillin binding proteins (PBPs). Its primary target is considered to be PBP3, which is important in cross-linking peptidoglycan molecules in bacteria cell walls. Wandara IM/IV Injection 1 gm/vial also binds to PBPs in some Gram-negative bacteria, and can inhibit both cell wall synthesis and some enzymes, such as DNA gyrase.

How Long Does It Take to Work?

Wandara IM/IV Injection 1 gm/vial begins to work within a few hours against susceptible organisms. The full therapeutic effects may take several days. In acute infections, improvement may be seen within 48 hours.

Absorption

Wandara IM/IV Injection 1 gm/vial is rapidly and completely absorbed after administration by the intramuscular or intravenous route.

Route of Elimination

Wandara IM/IV Injection 1 gm/vial is primarily eliminated via the kidneys. About 50% of an administered dose is eliminated unchanged in the urine, but the remainder is metabolized to inactive metabolites. It is rapidly excreted, with a half-life of 1-3 hours.

Dosage

Adults (>12 years): 1 gm given once a day.

Pediatric (3 months to 12 years): 15 mg/kg twice daily (not to exceed 1 g/day).

Ertapenem may be administered by IV infusion or IM injection. When administered intravenously, it should be infused over a period of 30 minutes.

IM administration of Ertapenem may be used as an alternative to IV administration in the treatment of those infections for which intramuscular therapy is appropriate.

The usual duration of therapy with Ertapenem is 3 to 14 days but varies by the type of infection and causative pathogen(s). When clinically indicated, a switch to an appropriate oral antimicrobial maybe implemented if clinical improvement has been observed.

Prophylaxis of surgical site infection following elective colorectal surgery: To prevent surgical site infections following surgery in adults, the recommended dosage is 1 g IV administered as a single intravenous dose given 1 hour prior to the surgical incision.

Patients with renal insufficiency: Ertapenem may be used for the treatment of infections in adult patients with renal insufficiency. In patients whose creatinine clearance is >30 mL/min no dosage adjustment is necessary. Adult patients with advanced renal insufficiency (creatinine clearance ≤30 mL/min), including those on haemodialysis, should receive 500 mg daily.

There are no data in paediatric patients with renal insufficiency.

Patients on Haemodialysis: If Ertapenem is given at least 6 hours prior to haemodialysis, no supplementary dose is needed. When adult patients on haemodialysis are given Ertapenem within 6 hours prior to haemodialysis, a supplementary 30% dose is recommended following the haemodialysis session. There are no data in patients undergoing peritoneal dialysis or haemofiltration. There are no data in paediatric patients on haemodialysis.

No dosage adjustment is recommended in patients with impaired hepatic function

The dosage and duration of ertapenem therapy differs on the indication. The recommended dosage for bacterial infections of the skin and structures is 1 g, administered once daily. For intra-abdominal infections, the recommended dose is 1 g administered once daily. For gynecologic infections, the dosage is 1 g, administered once daily. For pneumonia, the dose is 500 mg, administered every twelve hours. For urinary tract infections, the recommended dosage is 1 g administered once daily.

Administration

Wandara IM/IV Injection 1 gm/vial is typically administered intravenously or intramuscularly. It should be administered slowly by intravenous infusion over 30 minutes. It can also be given by deep intramuscular injection.

Side Effects

The most common side effects of ertapenem are nausea, headache, diarrhea, dizziness, and injection site reactions. Other side effects include rash, pruritus, urticaria, and anaphylaxis.

Toxicity

Wandara IM/IV Injection 1 gm/vial has a wide therapeutic range, and is generally regarded as safe. In rare cases, an overdose of ertapenem can lead to renal toxicity, hypotension, and seizures.

Precautions

Patients should be monitored for signs of gastrointestinal ulceration and bleeding while receiving ertapenem. ertapenem should also be used with caution in patients with history of allergic reactions to beta-lactam antibiotics, including penicillins and cephalosporins. ertapenem should also not be used to treat infections caused by viruses.

Interactions

Wandara IM/IV Injection 1 gm/vial may interact with other medications, including anticoagulants, quinolones, and immunosuppressants. Wandara IM/IV Injection 1 gm/vial should not be used with probenecid or drugs that block penicillin binding proteins. Patients should speak to their doctor or pharmacist before starting ertapenem to avoid interactions.

Disease Interactions

Wandara IM/IV Injection 1 gm/vial can worsen certain medical conditions and should not be used in patients with pre-existing kidney disease or electrolyte disturbances. ertapenem can also cause hyperkalemia, so patients with renal dysfunction or kidney disease should be closely monitored while taking ertapenem.

Drug Interactions

Wandara IM/IV Injection 1 gm/vial may interact with other medications. Some medications may increase or decrease the availability of ertapenem, leading to increased or decreased drug levels in the body. Additionally, certain medications may increase the risk of side effects such as seizures or renal toxicity. Patients should speak to their doctor or pharmacist before taking ertapenem.

Food Interactions

Wandara IM/IV Injection 1 gm/vial should be taken at least two hours before or after meals. Taking ertapenem with food may decrease its absorption and effectiveness.

Pregnancy Use

Wandara IM/IV Injection 1 gm/vial has not been studied in pregnant women. It is not known if ertapenem is safe during pregnancy; however, it may be used for pregnant women if the benefits outweigh the risks.

Lactation Use

Wandara IM/IV Injection 1 gm/vial has not been studied in breastfeeding women. It is not known if ertapenem is safe during breastfeeding; however, it may be used for breastfeeding women if the benefits outweigh the risks.

Acute Overdose

An acute overdose of ertapenem may lead to seizures, hypotension, and renal toxicity. Treatment for an overdose is supportive, and immediate medical attention is recommended.

Contraindication

Wandara IM/IV Injection 1 gm/vial should not be used in patients who are hypersensitive to it or to other carbapenems or penicillins. Additionally, ertapenem should not be used to treat infections caused by viruses.

Use Directions

Wandara IM/IV Injection 1 gm/vial should be taken as directed by your doctor and on the dosage invoice provided. Missing doses should be taken as soon as possible. In case of an overdose, seek immediate medical attention.

Storage Condition

Wandara IM/IV Injection 1 gm/vial should be stored at room temperature, away from heat and moisture. Keep the medication in a tightly closed container.

Volume of Distribution

The volume of distribution of ertapenem is 0.6-0.9 L/kg.

Half Life

The half-life of ertapenem is 1-3 hours.

Clearance

The clearance of ertapenem in adults is 13-18 mL/min/kg.

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Dr. Md. Nazrul Islam Shaheen

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