Triamcinolone Ace 40mg/ml Inj, 10ml

Manufacturer TEVA PARENTERAL MEDICINES Active Ingredient Triamcinolone Injection(trye am SIN oh lone) Pronunciation trye-am-SIN-oh-lone
It is used to treat arthritis of the knee.It is used for many health problems like allergy signs, asthma, adrenal gland problems, blood problems, skin rashes, or swelling problems. This is not a list of all health problems that this drug may be used for. Talk with the doctor.
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Drug Class
Corticosteroid
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Pharmacologic Class
Glucocorticoid
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Pregnancy Category
Category C
FDA Approved
Jan 1957
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DEA Schedule
Not Controlled

Overview

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What is this medicine?

Triamcinolone acetonide injection is a type of steroid medicine used to reduce inflammation and suppress the immune system. It's given as an injection into a joint, muscle, or skin lesion to treat conditions like arthritis, allergies, skin problems, and asthma.
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How to Use This Medicine

Taking Your Medication

To use this medication correctly, follow your doctor's instructions and read all the information provided. It is essential to follow the instructions carefully.

Administration

This medication can be administered in two ways:
- As an injection into the knee, as directed by your doctor.
- As a shot for other indications, also as directed by your doctor.

Storage and Disposal

If you need to store this medication at home, consult with your doctor, nurse, or pharmacist for guidance on proper storage.

Missed Dose

If you miss a dose, contact your doctor to determine the best course of action.
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Lifestyle & Tips

  • Report any signs of infection immediately (fever, chills, sore throat).
  • Avoid exposure to people with chickenpox or measles if you haven't had them or been vaccinated.
  • Do not stop the medication suddenly if you've been on it for a long time, as this can cause withdrawal symptoms. Your doctor will guide you on tapering.
  • Maintain a balanced diet, potentially low in sodium and high in potassium, as advised by your doctor.
  • Monitor blood sugar if you have diabetes or are at risk.
  • Carry a steroid warning card if on long-term systemic therapy.

Dosing & Administration

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Adult Dosing

Standard Dose: Varies significantly by indication and route of administration (e.g., intra-articular, intramuscular, intralesional). Not for intravenous use.
Dose Range: 2.5 - 100 mg

Condition-Specific Dosing:

intraArticularLargeJoints: 20-100 mg (e.g., knee, hip)
intraArticularSmallJoints: 2.5-5 mg (e.g., finger, toe)
intramuscularSystemic: 40-80 mg, deep IM into gluteal muscle, repeated every 2-4 weeks as needed
intralesional: 1 mg/injection site, not to exceed 1 mg/cm² of skin, total dose 1-30 mg
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Pediatric Dosing

Neonatal: Not established
Infant: Not established
Child: Dosing is highly individualized based on condition and route. For systemic IM use, doses typically range from 0.03-0.2 mg/kg every 1-7 days. Intra-articular doses are scaled down from adult doses.
Adolescent: Similar to adult dosing, individualized based on condition and route.
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Dose Adjustments

Renal Impairment:

Mild: No specific adjustment recommended
Moderate: No specific adjustment recommended
Severe: No specific adjustment recommended
Dialysis: Not significantly dialyzable; no specific adjustment recommended.

Hepatic Impairment:

Mild: No specific adjustment recommended
Moderate: No specific adjustment recommended
Severe: No specific adjustment recommended
Confidence: Medium

Pharmacology

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Mechanism of Action

Triamcinolone acetonide is a synthetic corticosteroid with potent anti-inflammatory and immunosuppressive properties. It acts by binding to intracellular glucocorticoid receptors, forming a complex that translocates to the nucleus and modulates gene expression. This leads to the synthesis of anti-inflammatory proteins (e.g., lipocortins) and inhibition of pro-inflammatory mediators (e.g., prostaglandins, leukotrienes, cytokines). It also suppresses the immune response by inhibiting the function of lymphocytes and macrophages.
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Pharmacokinetics

Absorption:

Bioavailability: Varies by route; systemic absorption occurs after local injection (e.g., intra-articular, intralesional, intramuscular).
Tmax: Intramuscular: 8-24 hours (for systemic effect)
FoodEffect: Not applicable for injectable formulation.

Distribution:

Vd: Not precisely quantified for triamcinolone acetonide, but generally distributed widely.
ProteinBinding: Approximately 60-70% (primarily to albumin and transcortin)
CnssPenetration: Limited, but can cross the blood-brain barrier.

Elimination:

HalfLife: Biological half-life (duration of action) is prolonged (18-36 hours) compared to plasma half-life (2-3 hours).
Clearance: Primarily hepatic metabolism and renal excretion.
ExcretionRoute: Urine (metabolites), small amount in feces.
Unchanged: <10%
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Pharmacodynamics

OnsetOfAction: Intra-articular: Within hours to 1 day; Intramuscular: Within 24-48 hours for systemic effects.
PeakEffect: Intra-articular: 1-2 days; Intramuscular: 1-2 days.
DurationOfAction: Intra-articular: Weeks to months; Intramuscular: 2-4 weeks (for systemic effects).
Confidence: Medium

Safety & Warnings

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Side Effects

Serious Side Effects: Seek Medical Help Immediately

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 medical attention right away:

Signs of an allergic reaction: rash, hives, itching, red, swollen, blistered, or peeling skin (with or without fever), wheezing, tightness in the chest or throat, difficulty breathing, swallowing, or talking, unusual hoarseness, or swelling of the mouth, face, lips, tongue, or throat. In rare cases, allergic reactions can be fatal.
Signs of infection: fever, chills, severe sore throat, ear or sinus pain, cough, increased or changed sputum production, painful urination, mouth sores, or a wound that won't heal.
Signs of Cushing's syndrome: weight gain in the upper back or abdomen, moon face, severe headache, or slow wound healing.
Signs of adrenal insufficiency: severe nausea or vomiting, severe dizziness or fainting, muscle weakness, fatigue, mood changes, decreased appetite, or weight loss.
Signs of high blood sugar: confusion, drowsiness, increased thirst or hunger, frequent urination, flushing, rapid breathing, or fruity-smelling breath.
Signs of high blood pressure: severe headache or dizziness, fainting, or changes in vision.
Signs of low potassium levels: muscle pain or weakness, muscle cramps, or an irregular heartbeat.
Signs of pancreatitis: severe abdominal pain, severe back pain, or severe nausea and vomiting.
Shortness of breath, significant weight gain, or swelling in the arms or legs.
Abnormal heartbeat (fast, slow, or irregular).
Chest pain.
Stomach pain, black, tarry, or bloody stools, vomiting blood, or coffee ground-like vomit.
Unexplained bruising or bleeding.
Bone pain.
Joint pain or swelling.
Muscle pain or weakness.
Fatigue or weakness.
Redness or white patches in the mouth or throat.
Changes in vision.
New or worsening mental, mood, or behavioral changes.
Changes in menstrual periods.
Seizures.
Skin changes (acne, stretch marks, slow healing, hair growth).
Purple, red, blue, brown, or black bumps or patches on the skin or in the mouth.
Burning, numbness, or tingling sensations.
Redness or swelling at the injection site.

Other Side Effects

Like all medications, this drug can cause side effects. Many people experience no side effects or only mild ones. If you're bothered by any of the following side effects or if they persist, contact your doctor:

Difficulty sleeping.
Nausea or vomiting.
Weight gain.
Restlessness.
Excessive sweating.
Hair thinning.

This is not an exhaustive list of possible side effects. If you have questions or concerns about side effects, consult your doctor. You can also report side effects to the FDA at 1-800-332-1088 or online at https://www.fda.gov/medwatch.
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Seek Immediate Medical Attention If You Experience:

  • Severe allergic reaction (rash, hives, swelling of face/lips/tongue, difficulty breathing)
  • Signs of infection (fever, chills, body aches, persistent cough, unusual discharge)
  • Severe stomach pain, black/tarry stools, or vomiting blood
  • Unusual weight gain, swelling in hands/ankles/feet
  • Extreme mood changes, depression, or suicidal thoughts
  • Muscle weakness or severe fatigue
  • Vision changes (blurred vision, eye pain)
  • Persistent high blood sugar symptoms (increased thirst, urination, hunger)
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Before Using This Medicine

Before Taking This Medication: Important Information to Share with Your Doctor

To ensure safe treatment, inform your doctor about the following:

Any allergies you have to this medication, its components, or other substances, including foods and drugs. Describe the allergic reaction you experienced, such as symptoms and signs.
Stomach or bowel problems, including diverticulitis, diverticulosis, ulcerative colitis, or ulcers.
Any current infections, including bacterial, viral, or fungal infections, as well as specific conditions like:
+ Amoeba infection (e.g., traveler's diarrhea)
+ Herpes infection of the eye
+ Malaria infection in the brain
+ Threadworm infestation
+ Other infections
If you have an infection at the site where the injection will be administered (for intramuscular injections).
If you have idiopathic thrombocytopenic purpura (ITP), a bleeding disorder (for intramuscular injections).

Additionally, provide your doctor and pharmacist with a comprehensive list of:

All prescription and over-the-counter (OTC) medications you are taking
Natural products and vitamins you are using
Any health problems you have

It is crucial to verify that this medication is safe to take with all your other medications and health conditions. Do not initiate, stop, or adjust the dosage of any medication without consulting your doctor.
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Precautions & Cautions

It is essential to inform all your healthcare providers, including doctors, nurses, pharmacists, and dentists, that you are taking this medication. Your doctor will likely recommend regular blood tests to monitor your condition. If you are taking this medication long-term, you may also need to have your eye pressure and bone density checked.

This medication may interfere with allergy skin tests, so be sure to notify your doctor and laboratory personnel that you are taking it. You may need to reduce your salt intake and increase your potassium consumption; consult with your doctor for personalized advice. If you have diabetes, it is crucial to closely monitor your blood sugar levels.

Before receiving any vaccinations, discuss the potential risks and benefits with your doctor, as some vaccines may not be effective or may increase the risk of infection when taken with this medication. If you have not previously had chickenpox or measles, avoid exposure to these illnesses, as they can be severe or even fatal in people taking steroid medications like this one. If you have been exposed, notify your doctor immediately.

Steroid medications, including this one, can increase the risk of infection, which can be mild or severe, and even life-threatening. The risk of infection is typically higher with higher doses of steroids. To minimize the risk of infection, practice good hygiene by washing your hands frequently, and avoid close contact with people who have infections, colds, or flu. If you experience any signs of infection, such as fever, chills, or sore throat, notify your doctor promptly.

In some cases, this medication can reactivate latent infections, including tuberculosis and hepatitis B. Inform your doctor if you have a history of these infections.

This medication may decrease the natural production of steroids in your body. If you experience stress, such as a fever, infection, surgery, or injury, consult with your doctor, as you may require additional oral steroids to help your body cope. Carry a warning card indicating that you may need extra steroids in certain situations.

Using this medication epidurally (injecting it into the spine) has been associated with severe and potentially life-threatening complications, including paralysis, loss of vision, stroke, and death. This use is not approved, and you should discuss the risks and benefits with your doctor.

If you are 65 or older, use this medication with caution, as you may be more susceptible to side effects. If you have been taking this medication for an extended period, consult with your doctor before stopping, as you may need to taper off the medication gradually. If you experience symptoms such as fatigue, weakness, shakiness, rapid heartbeat, confusion, sweating, or dizziness after missing a dose or stopping the medication, notify your doctor promptly.

Long-term use of this medication may increase the risk of osteoporosis (weak bones) and eye problems, such as cataracts or glaucoma. Discuss your individual risk factors and any concerns with your doctor.

Some formulations of this medication contain benzyl alcohol, which can be harmful to newborns and infants. If possible, avoid products containing benzyl alcohol in these age groups, and consult with your doctor for alternative options.

Prolonged use of this medication has been associated with an increased risk of Kaposi's sarcoma, a type of cancer. Discuss this risk with your doctor.

In children and adolescents, this medication may affect growth and development. Regular growth checks may be necessary; consult with your doctor for guidance.

If you are pregnant, plan to become pregnant, or are breastfeeding, discuss the potential benefits and risks of this medication with your doctor to ensure the best possible outcome for you and your baby.
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Overdose Information

Overdose Symptoms:

  • Acute overdose is rare but may include: severe fluid retention, hypertension, hyperglycemia, and electrolyte imbalances. Chronic overdose can lead to Cushing's syndrome symptoms (moon face, buffalo hump, striae, muscle wasting).

What to Do:

Seek immediate medical attention or call Poison Control at 1-800-222-1222. Treatment is supportive and symptomatic.

Drug Interactions

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Major Interactions

  • Live or live attenuated vaccines (risk of disseminated infection)
  • Strong CYP3A4 inducers (e.g., rifampin, phenytoin, barbiturates - decreased corticosteroid effect)
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, ritonavir - increased corticosteroid effect)
  • Anticoagulants (e.g., warfarin - altered anticoagulant effect, monitor INR)
  • NSAIDs (increased risk of GI ulceration/bleeding)
  • Diuretics (potassium-depleting, e.g., thiazides, loop diuretics - increased risk of hypokalemia)
  • Digitalis glycosides (increased risk of arrhythmias with hypokalemia)
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Moderate Interactions

  • Oral contraceptives/estrogens (may increase corticosteroid effects)
  • Antidiabetic agents (may increase blood glucose, requiring dose adjustment)
  • Cholestyramine (may decrease corticosteroid absorption)
  • Cyclosporine (mutual inhibition of metabolism, increased levels of both drugs)
  • Neuromuscular blocking agents (prolonged blockade with high-dose corticosteroids)
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Minor Interactions

  • Antacids (may decrease absorption if given orally, but this is an injectable)
  • Grapefruit juice (potential for increased systemic exposure, though less significant for injectables)

Monitoring

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Baseline Monitoring

Blood pressure

Rationale: Corticosteroids can cause hypertension.

Timing: Before initiation

Blood glucose

Rationale: Corticosteroids can cause hyperglycemia.

Timing: Before initiation

Electrolytes (especially potassium)

Rationale: Risk of hypokalemia.

Timing: Before initiation

Weight

Rationale: Fluid retention and weight gain are common side effects.

Timing: Before initiation

Ophthalmic exam (if long-term use)

Rationale: Risk of cataracts and glaucoma.

Timing: Before initiation of long-term therapy

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Routine Monitoring

Blood pressure

Frequency: Regularly during therapy, especially with systemic use

Target: Normal range for patient

Action Threshold: Significant elevation requiring intervention

Blood glucose

Frequency: Regularly, especially in diabetics or with systemic use

Target: Individualized, typically <140 mg/dL fasting

Action Threshold: Persistent hyperglycemia

Electrolytes (especially potassium)

Frequency: Periodically, especially with concomitant diuretics or cardiac conditions

Target: 3.5-5.0 mEq/L

Action Threshold: Hypokalemia (<3.5 mEq/L)

Growth and development (pediatric patients)

Frequency: Regularly

Target: Normal growth curve

Action Threshold: Growth suppression

Signs of infection

Frequency: Continuously

Target: Absence of infection

Action Threshold: Fever, malaise, localized signs of infection

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Symptom Monitoring

  • Signs of infection (fever, sore throat, malaise)
  • Unusual bruising or bleeding
  • Swelling in ankles or feet
  • Increased thirst or urination
  • Muscle weakness or pain
  • Mood changes (depression, euphoria, insomnia)
  • Vision changes
  • Stomach pain or black/tarry stools
  • Slow wound healing

Special Patient Groups

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Pregnancy

Category C. Use during pregnancy only if the potential benefit justifies the potential risk to the fetus. Animal studies have shown teratogenic effects. Systemic corticosteroids can cross the placenta.

Trimester-Specific Risks:

First Trimester: Potential for teratogenicity (e.g., cleft palate) observed in animal studies, though human data are limited and conflicting.
Second Trimester: Risk of fetal growth restriction, adrenal suppression.
Third Trimester: Risk of fetal growth restriction, adrenal suppression, especially with prolonged use. Neonates should be monitored for signs of hypoadrenalism.
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Lactation

L3 (Moderately Safe). Corticosteroids are excreted in breast milk. Low doses are generally considered compatible with breastfeeding. High doses or prolonged use may cause infant adrenal suppression or growth retardation. Monitor infant for adverse effects.

Infant Risk: Low risk with typical therapeutic doses; higher risk with prolonged high-dose systemic therapy.
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Pediatric Use

Children are more susceptible to growth retardation and suppression of the hypothalamic-pituitary-adrenal (HPA) axis. Monitor growth and development carefully. Intra-articular injections should be used cautiously in children due to potential effects on growth plates.

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Geriatric Use

Elderly patients may be more susceptible to adverse effects such as osteoporosis, hypertension, diabetes, and fluid retention. Use the lowest effective dose for the shortest duration possible. Monitor closely for side effects.

Clinical Information

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Clinical Pearls

  • Triamcinolone acetonide injectable suspension is NOT for intravenous, intrathecal, epidural, or ophthalmic use. Serious adverse events, including death, have been reported with these routes.
  • Shake the vial well before drawing up the dose to ensure uniform suspension.
  • Local injections (intra-articular, intralesional) can still lead to systemic absorption and side effects.
  • Patients on long-term systemic corticosteroids should not abruptly discontinue the drug due to risk of adrenal insufficiency.
  • Protect the injection site from infection. Aseptic technique is crucial.
  • Warn patients about potential mood changes, including depression or euphoria.
  • Consider calcium and vitamin D supplementation for patients on long-term systemic therapy to mitigate osteoporosis risk.
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Alternative Therapies

  • Other injectable corticosteroids (e.g., methylprednisolone acetate, betamethasone)
  • Oral corticosteroids (e.g., prednisone, dexamethasone)
  • NSAIDs (for inflammatory conditions)
  • Disease-modifying antirheumatic drugs (DMARDs) or biologics (for chronic inflammatory conditions)
  • Physical therapy
  • Topical corticosteroids (for skin conditions)
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Cost & Coverage

Average Cost: $50 - $200 per 10ml vial (40mg/ml)
Generic Available: Yes
Insurance Coverage: Tier 1 or Tier 2 (Generic), Tier 3 (Brand)
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General Drug Facts

If your symptoms or health problems persist or worsen, it is essential to contact your doctor for further guidance. To ensure safe use, never share your medication with others, and do not take medication prescribed to someone else. Store all medications in a secure location, out of reach of children and pets, to prevent accidental ingestion. Dispose of unused or expired medications properly; do not flush them down the toilet or pour them down the drain unless instructed to do so by a healthcare professional. If you are unsure about the correct disposal method, consult your pharmacist, who can also inform you about potential drug take-back programs in your area. Some medications may come with an additional patient information leaflet, which your pharmacist can provide. If you have any questions or concerns about your medication, discuss them with your doctor, nurse, pharmacist, or other healthcare provider. In the event of a suspected overdose, immediately contact your local poison control center or seek medical attention. Be prepared to provide information about the medication taken, the amount, and the time of ingestion.