Pfizerpen G 5mu Inj, 1 Vial
Overview
What is this medicine?
How to Use This Medicine
To ensure safe and effective use, take this medication exactly as directed by your doctor. Carefully read all accompanying information and follow the instructions provided. This medication is administered either as an intramuscular injection or as an intravenous infusion, which is given over a specified period of time.
Storing and Disposing of Your Medication
If you need to store this medication at home, consult with your doctor, nurse, or pharmacist to determine the appropriate storage method.
Missing a Dose
If you miss a dose, contact your doctor immediately to receive guidance on the next steps to take.
Lifestyle & Tips
- Complete the entire course of medication as prescribed, even if you start to feel better. Stopping early can lead to the infection returning and bacteria becoming resistant to the antibiotic.
- Report any signs of an allergic reaction (e.g., rash, itching, swelling, difficulty breathing) immediately to your healthcare provider.
- Inform your healthcare provider about all other medications you are taking, including over-the-counter drugs, herbal supplements, and vitamins, to avoid potential drug interactions.
Available Forms & Alternatives
Available Strengths:
Dosing & Administration
Adult Dosing
Condition-Specific Dosing:
Pediatric Dosing
Dose Adjustments
Renal Impairment:
Hepatic Impairment:
Pharmacology
Mechanism of Action
Pharmacokinetics
Absorption:
Distribution:
Elimination:
Pharmacodynamics
Safety & Warnings
Side Effects
Although rare, some people may experience severe and potentially life-threatening side effects while taking this medication. If you notice any of the following symptoms, contact your doctor or seek immediate medical attention:
Signs of an allergic reaction, such as:
+ Rash
+ Hives
+ Itching
+ Red, swollen, blistered, or peeling skin (with or without fever)
+ Wheezing
+ Tightness in the chest or throat
+ Trouble breathing, swallowing, or talking
+ Unusual hoarseness
+ Swelling of the mouth, face, lips, tongue, or throat
Note: In rare cases, allergic reactions can be fatal.
Signs of high potassium levels, including:
+ Abnormal heartbeat
+ Confusion
+ Weakness, lightheadedness, or dizziness
+ Feeling like passing out
+ Numbness or tingling
+ Shortness of breath
Severe dizziness or fainting
Fever, chills, or sore throat
Unexplained bruising or bleeding
Feeling extremely tired or weak
Chest pain or pressure
Headache
Rapid heartbeat
Fast breathing
Flushing
Yellowing of the skin or eyes
Muscle or joint pain
Stomach pain
Twitching
Seizures
Difficulty urinating or changes in urine output
Diarrhea (common with antibiotics), especially if it's severe, watery, or bloody (may be a sign of C. diff-associated diarrhea, a potentially life-threatening condition)
If you experience any of these symptoms, contact your doctor immediately.
Additional Side Effects of This Medication
While many people may not experience side effects or only have mild ones, it's essential to be aware of the following possible side effects:
Diarrhea
Upset stomach or vomiting
Mouth irritation or mouth sores
Change in tongue color
* Irritation at the injection site (if administered via muscle injection)
If you're concerned about any side effects or if they persist, contact your doctor for guidance.
Reporting Side Effects
If you experience any side effects, you can report them to the FDA at 1-800-332-1088 or online at https://www.fda.gov/medwatch. Your doctor can also provide advice on managing side effects.
Seek Immediate Medical Attention If You Experience:
- Severe allergic reaction (anaphylaxis): difficulty breathing, swelling of face/throat, rapid heartbeat, dizziness, severe rash.
- Severe or persistent diarrhea, especially if bloody or watery (may indicate Clostridioides difficile-associated diarrhea).
- Unusual bleeding or bruising.
- Signs of superinfection: new or worsening fever, sore throat, oral thrush (white patches in mouth), vaginal yeast infection (itching, discharge).
Before Using This Medicine
It is essential to inform your doctor about the following:
Any allergies you have, including allergies to this medication, its components, or other substances, such as foods or drugs. Be sure to describe the allergic reaction you experienced, including any symptoms that occurred.
If you are currently taking any of the following medications:
+ Chloramphenicol
+ Erythromycin
+ Sulfonamides (e.g., sulfamethoxazole)
+ Tetracyclines (e.g., doxycycline)
If you are unsure about any of these medications, consult with your doctor or pharmacist.
Please note that this is not an exhaustive list of all potential interactions with this medication. To ensure your safety, it is crucial to:
Inform your doctor and pharmacist about all medications you are taking, including:
+ Prescription medications
+ Over-the-counter (OTC) medications
+ Natural products
+ Vitamins
Share information about any existing health problems.
Verify that it is safe to take this medication with all your other medications and health conditions.
Never start, stop, or change the dose of any medication without first consulting your doctor.
Precautions & Cautions
Do not exceed the prescribed duration of treatment, as this may increase the risk of a second infection. High doses of this medication can lead to severe and potentially life-threatening electrolyte imbalances. Discuss any concerns with your doctor.
If you have diabetes and regularly test your urine glucose levels, consult your doctor to determine the most suitable testing methods to use while taking this medication. Additionally, inform your doctor and laboratory personnel that you are taking this drug, as it may affect the results of certain lab tests.
If you are following a low-sodium or low-potassium diet, discuss this with your doctor to ensure safe treatment. Be aware that this medication can cause severe skin reactions, including Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and other serious conditions that may also affect internal organs. These reactions can be fatal. Seek immediate medical attention if you experience symptoms such as red, swollen, blistered, or peeling skin; red or irritated eyes; sores in your mouth, throat, nose, eyes, genitals, or other areas of skin; fever; chills; body aches; shortness of breath; or swollen glands.
When administering this medication to newborns, exercise caution, as the risk of side effects may be higher in this age group. If you are pregnant, plan to become pregnant, or are breastfeeding, inform your doctor to discuss the potential benefits and risks to you and your baby.
Overdose Information
Overdose Symptoms:
- Neurological toxicity (e.g., seizures, confusion, twitching, hyperreflexia), especially in patients with renal impairment or high doses.
- Electrolyte imbalances (e.g., hyperkalemia with potassium salt, hypernatremia with sodium salt).
- Nausea, vomiting, diarrhea.
What to Do:
Seek immediate medical attention or call a poison control center (1-800-222-1222). Treatment is supportive and symptomatic. Hemodialysis can remove penicillin G from the blood.
Drug Interactions
Major Interactions
- Methotrexate (increased methotrexate toxicity due to decreased renal clearance)
- Tetracyclines (may antagonize bactericidal effect of penicillin G)
Moderate Interactions
- Probenecid (increases penicillin G plasma concentrations and prolongs half-life by inhibiting renal tubular secretion)
- Oral contraceptives (theoretical reduction in efficacy, though clinical significance is debated)
- Aminoglycosides (physical incompatibility in solution; may inactivate aminoglycosides if mixed directly)
Monitoring
Baseline Monitoring
Rationale: Penicillin G is primarily renally eliminated; baseline assessment is crucial for dosing adjustments.
Timing: Prior to initiation of therapy
Rationale: High doses of potassium penicillin G can lead to hyperkalemia; sodium penicillin G can contribute to sodium overload.
Timing: Prior to initiation of therapy, especially with high doses
Routine Monitoring
Frequency: Daily, especially during the first few days of therapy
Target: Absence of symptoms
Action Threshold: Any sign of allergic reaction requires immediate discontinuation and management.
Frequency: Every 2-3 days or as clinically indicated, especially in patients with pre-existing renal impairment or receiving high doses.
Target: Stable or improving values
Action Threshold: Significant increase in BUN/creatinine may indicate nephrotoxicity or drug accumulation, requiring dose adjustment.
Frequency: Weekly or more frequently with high doses or in patients at risk for electrolyte imbalances.
Target: Within normal limits
Action Threshold: Hyperkalemia or hypernatremia may require dose adjustment or electrolyte management.
Frequency: Weekly for prolonged therapy (e.g., >2 weeks)
Target: Within normal limits
Action Threshold: Leukopenia, thrombocytopenia, or hemolytic anemia may occur with prolonged high-dose therapy.
Frequency: Daily throughout therapy and post-therapy
Target: Absence of symptoms
Action Threshold: Development of new infections requires appropriate diagnostic workup and treatment.
Symptom Monitoring
- Skin rash
- Hives
- Itching
- Swelling of face/lips/tongue/throat
- Difficulty breathing or swallowing
- Wheezing
- Severe diarrhea (especially if bloody or watery)
- Abdominal cramps
- Fever
- Sore throat
- Unusual bleeding or bruising
- Seizures (rare, with very high doses or renal impairment)
Special Patient Groups
Pregnancy
Penicillin G is generally considered safe for use during pregnancy (Pregnancy Category B). Studies in animals have not shown fetal harm, and adequate and well-controlled studies in pregnant women have not demonstrated a risk to the fetus. It is commonly used for infections like syphilis in pregnant women.
Trimester-Specific Risks:
Lactation
Penicillin G is excreted into breast milk in small amounts. It is generally considered compatible with breastfeeding. Monitor the infant for potential adverse effects such as diarrhea, candidiasis (thrush, diaper rash), or allergic reactions (e.g., rash).
Pediatric Use
Dosing must be carefully calculated based on weight, age, and the specific infection. Neonates and young infants have immature renal function, requiring lower doses and/or extended dosing intervals to prevent accumulation and toxicity. Close monitoring for adverse effects is essential.
Geriatric Use
Elderly patients are more likely to have decreased renal function, which can lead to reduced clearance and increased plasma concentrations of penicillin G. Dose adjustments based on creatinine clearance are often necessary. Monitor for signs of neurotoxicity and electrolyte imbalances.
Clinical Information
Clinical Pearls
- Always confirm penicillin allergy status before administration. A history of penicillin allergy should be thoroughly investigated, as many reported allergies are not true IgE-mediated reactions.
- For severe infections, continuous IV infusion of penicillin G can maintain more consistent therapeutic drug levels and may be preferred over intermittent boluses.
- High doses of potassium penicillin G can lead to significant potassium load, especially in patients with renal impairment, requiring electrolyte monitoring.
- Penicillin G is not effective against beta-lactamase producing bacteria, including many strains of Staphylococcus aureus and Gram-negative bacilli.
- Ensure proper administration technique for IM injections (deep IM) to minimize pain and local reactions.
Alternative Therapies
- Other beta-lactam antibiotics (e.g., ampicillin, amoxicillin, cefazolin, ceftriaxone)
- Macrolides (e.g., azithromycin, erythromycin) for penicillin-allergic patients or specific infections
- Vancomycin (for resistant Gram-positive infections, e.g., MRSA)
- Clindamycin (for anaerobic infections or certain Gram-positive infections in penicillin-allergic patients)