Hyaluronidase – Uses, Dosage, Side Effects, Interaction

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Hyaluronidase - Uses, Dosage, Side Effects, Interaction
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Hyaluronidase is an injectable enzyme with potential adjuvant activity. Upon subcutaneous administration, hyaluronidase modifies the permeability of connective tissue by hydrolyzing hyaluronic acid. This temporarily decreases interstitial viscosity and allows drugs that are co-injected to spread rapidly through the interstitial space, thereby facilitating absorption and/or...

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Article Summary

Hyaluronidase is an injectable enzyme with potential adjuvant activity. Upon subcutaneous administration, hyaluronidase modifies the permeability of connective tissue by hydrolyzing hyaluronic acid. This temporarily decreases interstitial viscosity and allows drugs that are co-injected to spread rapidly through the interstitial space, thereby facilitating absorption and/or distribution of the co-injected agents. Hyaluronidase is an enzyme used to improve the absorption and dispersion of parenterally administered fluids,...

Key Takeaways

  • This article explains Mechanism of Action in simple medical language.
  • This article explains Indications in simple medical language.
  • This article explains Contraindications in simple medical language.
  • This article explains Dosage in simple medical language.
Educational health guideWritten for patient understanding and clinical awareness.
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Mechanism of Action

Hyaluronidase cleaves hyaluronic acid at the glucosaminidic bond between C1 of glucosamine and C4 of glucuronic acid. Hyaluronic acid is a key component of the extracellular matrix. Injection of hyaluronidase with other fluids, drugs, or radiopaque agents improves the ability of these other compounds to permeate the extracellular space more easily.

Indications

  • Hyaluronidase is indicated for subcutaneous fluid administration for hydration and increasing resorption of radiopaque agents in subcutaneous urography. Hyaluronidase is also indicated by multiple routes to increase the dispersion of other injectable drugs.
  • Hyaluronidase is indicated for subcutaneous fluid administration for hydration and increasing resorption of radiopaque agents in subcutaneous urography. Hyaluronidase is also indicated by multiple routes to increase the dispersion of other injectable drugs.
  • As an adjuvant in subcutaneous fluid administration (hypodermoclysis) for achieving hydration.
  • As an adjuvant in subcutaneous urography for improving the resorption of radiopaque agents
  • Hyaluronidase is an enzyme used to improve the absorption and dispersion of parenterally administered fluids, drugs, and contrast agents
  • Parenteral rehydration therapy
  • Parenteral drug administration
  • Subcutaneous urography

FDA Approved Indications

  • Absorption and dispersion enhancer of injected drugs
  • Subcutaneous fluid administration for hydration therapy – hypodermoclysis
  • Subcutaneous urography to improve absorption of radiopaque agents

Non-FDA Approved Uses

  • Extravasation of medications from intravenous lines management
  • Adjunct to local anesthetic eye blocks for ophthalmic surgery
  • Keloid scar treatment – involves cryosurgery followed by injections with hyaluronidase, triamcinolone, and 5-fluorouracil
  • Reversing cosmetic facial fillers composed of hyaluronic acid

Contraindications

  • Hyaluronidase hypersensitivity.
  • Extravasation, intravenous administration.
  • Ocular exposure, ocular surgery.
  • Infection.
  • Children, hypervolemia, infants.
  • Pregnancy.
  • Breast-feeding.
  • Viral infection.

Dosage

Strengths: 150 units; 1500 units; 150 units/mL; human recombinant 150 units/mL; 200 units/mL; 6200 units

Hypodermoclysis

  • After inserting the needle, begin clysis with the tip of the needle lying free and movable between the skin and muscle. The fluid should start in readily without pain or lump. Then hyaluronidase should be injected into the rubber tubing close to the needle.
  • Alternate method: Inject hyaluronidase under the skin before clysis. 150 to 200 units will facilitate the absorption of 1000 mL or more of the solution.
  • The dose, rate of injection, and type of solution should be individualized; the rate of infusion and volume of administration should not exceed those used for intravenous infusion.
  • Hypovolemia may occur if electrolyte-free solutions are given.
  • Adding adequate quantities of electrolytes and/or controlling the volume and rate of administration will prevent hypovolemia.

Subcutaneous Urography

  • With the patient prone, inject 75 Units subcutaneously over each scapula, followed by injection of contrast medium at the same sites

Hypodermoclysis

After inserting the needle, begin clysis with the tip of the needle lying free and movable between the skin and muscle. The fluid should start in readily without pain or lump. Then hyaluronidase should be injected into the rubber tubing close to the needle.

Alternate method: Inject hyaluronidase under the skin before clysis. 150 to 200 units will facilitate the absorption of 1000 mL or more of the solution.

Under 3 years of age:

  • Limit the volume of a single class to 200 mL

Premature Infants or During the Neonatal Period:

  • Maximum daily dosage: 25 mL/kg of body weight
  • The maximum rate of administration: 2 mL/minute
  • The dose, rate of injection, and type of solution should be individualized; the rate of infusion and volume of administration should not exceed those used for intravenous infusion.
  • Hypovolemia may occur if electrolyte-free solutions are given.
  • Adding adequate quantities of electrolytes and/or controlling the volume and rate of administration will prevent hypovolemia.

Pediatric Dose for Subcutaneous Urography

  • With the patient prone, inject 75 Units subcutaneously over each scapula, followed by injection of contrast medium at the same sites
  • As an adjuvant in subcutaneous urography for improving the resorption of radiopaque agents

Administration advice:

  • Do not give intravenously
  • For infiltration, interstitial, intramuscular, intraocular, peribulbar, retrobulbar, soft tissue, or subcutaneous use.

Side Effects

The Most Common

  • constipation
  • diarrhea
  • vomiting
  • nausea
  • stomach pain
  • loss of appetite
  • tiredness
  • pain in the head or upper neck. সহজ বাংলা: মাথাব্যথা।" data-rx-term="headache" data-rx-definition="Headache means pain in the head or upper neck. সহজ বাংলা: মাথাব্যথা।">headache
  • difficulty falling asleep or staying asleep
  • pain, burning, or tingling in the hands or feet
  • swelling of the hands, ankles, or feet
  • pain: Back pain means pain in the spine, muscles, discs, joints, or nerves of the back. সহজ বাংলা: পিঠ/কোমরের ব্যথা।" data-rx-term="back pain" data-rx-definition="Back pain means pain in the spine, muscles, discs, joints, or nerves of the back. সহজ বাংলা: পিঠ/কোমরের ব্যথা।">back pain
  • muscle spasms
  • itching, swelling, bruising, or redness of the skin at the injection site
  • unusual bruising or bleeding
  • pale skin, fatigue, or shortness of breath
  • fever, cough, or other signs of infection
  • yellow eyes or skin; dark urine; or pain or discomfort in right upper stomach area
  • chest pain, feeling faint, swollen legs, or shortness of breath (especially if you are being treated for amyloidosis)

More Common

  • Blurred vision
  • swelling in your hands, feet, or other body areas; or
  • pain, swelling, itching, or redness where the injection was given.
  • chills
  • confusion
  • dizziness, faintness, or lightheadedness when getting up suddenly from a lying or sitting position
  • fast, pounding, or irregular heartbeat or pulse
  • nausea or vomiting
  • redness of the skin
  • sweating
  • swelling
  • unusual tiredness or weakness
  • unusually warm skin

Rare

  • Cough
  • difficulty swallowing
  • dizziness
  • fast heartbeat
  • hives or welts
  • itching
  • large, hive-like swelling on the face, eyelids, lips, tongue, throat, hands, legs, feet, or sex organs
  • puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue
  • redness of the skin
  • skin rash
  • tightness in the chest
  • unusual tiredness or weakness

Drug Interaction

Pregnancy and Lactation

AU TGA pregnancy category: Exempt
US FDA pregnancy category: Not assigned

Pregnancy

Medications exempted from pregnancy classification are not absolutely safe for use in pregnancy in all circumstances. Some exempted medicines, for example, the complementary medicine, St John’s Wort, may interact with other medicines and induce unexpected adverse effects in the mother and/or fetus.

Lactation

Consider the developmental and health benefits of breastfeeding along with the mother’s clinical need for this medication as well as any potential adverse effects from this drug or the underlying maternal condition.

How should this medicine be used?

Daratumumab and hyaluronidase-fihj injection comes as a solution (liquid) to be injected subcutaneously (just under the skin) into the abdomen (stomach) over 3 to 5 minutes. The length of your treatment will depend on your condition and how well your body responds to treatment.

A doctor or nurse will watch you closely while you are receiving the medication and afterwards to be sure you are not having a serious reaction to the medication. You will be given other medications to help prevent and treat reactions to daratumumab and hyaluronidase-fihj before and after you receive your medication. Tell your doctor or nurse immediately if you experience any of the following symptoms: difficulty breathing or shortness of breath, chest pain, wheezing, throat tightness and irritation, cough, runny or stuffy nose, headache, itching, nausea, vomiting, fever, chills, rash, hives, blurred vision or other vision changes, or dizziness or lightheadedness.

Your doctor may temporarily or permanently stop your treatment. This depends on how well the medication works for you and the side effects you experience. Be sure to tell your doctor how you are feeling during your treatment with daratumumab and hyaluronidase-fihj. Ask your pharmacist or doctor for a copy of the manufacturer’s information for the patient. Ask your pharmacist or doctor for a copy of the manufacturer’s information for the patient.

What special precautions should I follow?

Before receiving daratumumab and hyaluronidase-fihj injection,

  • tell your doctor and pharmacist if you are allergic to daratumumab, hyaluronidase-fihj, any other medications, or any of the ingredients in daratumumab and hyaluronidase-fihj injection. Ask your pharmacist for a list of the ingredients.
  • tell your doctor and pharmacist what other prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking or plan to take. Your doctor may need to change the doses of your medications or monitor you carefully for side effects.
  • tell your doctor if you have or have ever had shingles (a painful rash that occurs after infection with herpes zoster or chickenpox), hepatitis B (a virus that infects the liver and may cause severe liver damage), glaucoma (a type of eye disease), high blood pressure, or breathing problems or a lung disease such as chronic obstructive pulmonary disease (COPD; a group of lung diseases, which includes chronic bronchitis and emphysema). If you are being treated for amyloidosis, tell your doctor if you have heart failure or heart disease.
  • tell your doctor if you are pregnant, plan to become pregnant, or are breastfeeding. You should use birth control to prevent pregnancy during your treatment with daratumumab and hyaluronidase-fihj and for at least 3 months after your final dose. Talk to your doctor about types of birth control that will work for you. If you become pregnant while receiving daratumumab and hyaluronidase-fihj injections, call your doctor.
  • if you are having surgery, including dental surgery, tell the doctor or dentist that you are receiving daratumumab and hyaluronidase-fihj injections.

References

  1. https://www.accessdata.fda.gov/drugsatfda_docs/nda/2005/021716s000_HydaseTOC.cfm
  2. https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/021859s009lbl.pdf
  3. https://www.cancer.gov/about-cancer/treatment/drugs/daratumumabandhyaluronidase-fihj
  4. https://en.wikipedia.org/wiki/Hyaluronidase
  5. https://go.drugbank.com/drugs/DB14740
  6. https://www.mayoclinic.org/drugs-supplements/hyaluronidase-injection-route-subcutaneous-route/side-effects/drg-20064183
  7. https://www.drugs.com/mtm/hyaluronidase-injection.html
  8. https://medlineplus.gov/druginfo/meds/a620040.html
  9. https://pubchem.ncbi.nlm.nih.gov/compound/Hyaluronidase
  10. PubChem

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    Follow up and return early if worse

    If symptoms worsen, new warning signs appear, or treatment is not helping, return for review quickly.

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Frequently Asked Questions

Mechanism of Action Hyaluronidase cleaves hyaluronic acid at the glucosaminidic bond between C1 of glucosamine and C4 of glucuronic acid. Hyaluronic acid is a key component of the extracellular matrix. Injection of hyaluronidase with other fluids, drugs, or radiopaque agents improves the ability of these other compounds to permeate the extracellular space more easily. Indications Hyaluronidase is indicated for subcutaneous fluid administration for hydration and increasing resorption of radiopaque agents in subcutaneous urography. Hyaluronidase is also indicated by multiple routes to increase the dispersion of other injectable drugs. Hyaluronidase is indicated for subcutaneous fluid administration for hydration and increasing resorption of radiopaque agents in subcutaneous urography. Hyaluronidase is also indicated by multiple routes to increase the dispersion of other injectable drugs. As an adjuvant in subcutaneous fluid administration (hypodermoclysis) for achieving hydration. As an adjuvant in subcutaneous urography for improving the resorption of radiopaque agents Hyaluronidase is an enzyme used to improve the absorption and dispersion of parenterally administered fluids, drugs, and contrast agents Parenteral rehydration therapy Parenteral drug administration Subcutaneous urography FDA Approved Indications Absorption and dispersion enhancer of injected drugs Subcutaneous fluid administration for hydration therapy - hypodermoclysis Subcutaneous urography to improve absorption of radiopaque agents Non-FDA Approved Uses Extravasation of medications from intravenous lines management Adjunct to local anesthetic eye blocks for ophthalmic surgery Keloid scar treatment – involves cryosurgery followed by injections with hyaluronidase, triamcinolone, and 5-fluorouracil Reversing cosmetic facial fillers composed of hyaluronic acid Contraindications Hyaluronidase hypersensitivity. Extravasation, intravenous administration. Ocular exposure, ocular surgery. Infection. Children, hypervolemia, infants. Pregnancy. Breast-feeding. Viral infection. Dosage Strengths: 150 units; 1500 units; 150 units/mL; human recombinant 150 units/mL; 200 units/mL; 6200 units Hypodermoclysis After inserting the needle, begin clysis with the tip of the needle lying free and movable between the skin and muscle. The fluid should start in readily without pain or lump. Then hyaluronidase should be injected into the rubber tubing close to the needle. Alternate method: Inject hyaluronidase under the skin before clysis. 150 to 200 units will facilitate the absorption of 1000 mL or more of the solution. The dose, rate of injection, and type of solution should be individualized; the rate of infusion and volume of administration should not exceed those used for intravenous infusion. Hypovolemia may occur if electrolyte-free solutions are given. Adding adequate quantities of electrolytes and/or controlling the volume and rate of administration will prevent hypovolemia. Subcutaneous Urography With the patient prone, inject 75 Units subcutaneously over each scapula, followed by injection of contrast medium at the same sites Hypodermoclysis After inserting the needle, begin clysis with the tip of the needle lying free and movable between the skin and muscle. The fluid should start in readily without pain or lump. Then hyaluronidase should be injected into the rubber tubing close to the needle. Alternate method: Inject hyaluronidase under the skin before clysis. 150 to 200 units will facilitate the absorption of 1000 mL or more of the solution. Under 3 years of age: Limit the volume of a single class to 200 mL Premature Infants or During the Neonatal Period: Maximum daily dosage: 25 mL/kg of body weight The maximum rate of administration: 2 mL/minute The dose, rate of injection, and type of solution should be individualized; the rate of infusion and volume of administration should not exceed those used for intravenous infusion. Hypovolemia may occur if electrolyte-free solutions are given. Adding adequate quantities of electrolytes and/or controlling the volume and rate of administration will prevent hypovolemia. Pediatric Dose for Subcutaneous Urography With the patient prone, inject 75 Units subcutaneously over each scapula, followed by injection of contrast medium at the same sites As an adjuvant in subcutaneous urography for improving the resorption of radiopaque agents Administration advice: Do not give intravenously For infiltration, interstitial, intramuscular, intraocular, peribulbar, retrobulbar, soft tissue, or subcutaneous use. Side Effects The Most Common constipation diarrhea vomiting nausea stomach pain loss of appetite tiredness headache difficulty falling asleep or staying asleep pain, burning, or tingling in the hands or feet swelling of the hands, ankles, or feet back pain muscle spasms itching, swelling, bruising, or redness of the skin at the injection site unusual bruising or bleeding pale skin, fatigue, or shortness of breath fever, cough, or other signs of infection yellow eyes or skin; dark urine; or pain or discomfort in right upper stomach area chest pain, feeling faint, swollen legs, or shortness of breath (especially if you are being treated for amyloidosis) More Common Blurred vision swelling in your hands, feet, or other body areas; or pain, swelling, itching, or redness where the injection was given. chills confusion dizziness, faintness, or lightheadedness when getting up suddenly from a lying or sitting position fast, pounding, or irregular heartbeat or pulse nausea or vomiting redness of the skin sweating swelling unusual tiredness or weakness unusually warm skin Rare Cough difficulty swallowing dizziness fast heartbeat hives or welts itching large, hive-like swelling on the face, eyelids, lips, tongue, throat, hands, legs, feet, or sex organs puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue redness of the skin skin rash tightness in the chest unusual tiredness or weakness Drug Interaction DRUG INTERACTION 1,2-Benzodiazepine The therapeutic efficacy of 1,2-Benzodiazepine can be decreased when used in combination with Hyaluronidase. Acetylsalicylic acid The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Acetylsalicylic acid. Amitriptyline The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Amitriptyline. Antazoline The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Antazoline. Aripiprazole The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Aripiprazole. Aripiprazole lauroxil The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Aripiprazole lauroxil. Articaine Hyaluronidase can cause an increase in the absorption of Articaine resulting in an increased serum concentration and potentially a worsening of adverse effects. Azelastine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Azelastine. Benzatropine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Benzatropine. Benzocaine Hyaluronidase can cause an increase in the absorption of Benzocaine resulting in an increased serum concentration and potentially a worsening of adverse effects. Benzyl alcohol Hyaluronidase can cause an increase in the absorption of Benzyl alcohol resulting in an increased serum concentration and potentially a worsening of adverse effects. Betamethasone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Betamethasone. Betamethasone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Betamethasone phosphate. Bethanidine The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Bethanidine. Brompheniramine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Brompheniramine. Bupivacaine Hyaluronidase can cause an increase in the absorption of Bupivacaine resulting in an increased serum concentration and potentially a worsening of adverse effects. Butacaine Hyaluronidase can cause an increase in the absorption of Butacaine resulting in an increased serum concentration and potentially a worsening of adverse effects. Butamben Hyaluronidase can cause an increase in the absorption of Butamben resulting in an increased serum concentration and potentially a worsening of adverse effects. Butriptyline The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Butriptyline. Cetirizine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Cetirizine. Chloroprocaine Hyaluronidase can cause an increase in the absorption of Chloroprocaine resulting in an increased serum concentration and potentially a worsening of adverse effects. Chlorpheniramine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Chlorpheniramine. Chlorpromazine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Chlorpromazine. Cimetidine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Cimetidine. Cinchocaine Hyaluronidase can cause an increase in the absorption of Cinchocaine resulting in an increased serum concentration and potentially a worsening of adverse effects. Clemastine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Clemastine. Clobetasol propionate The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Clobetasol propionate. Clonazepam The therapeutic efficacy of Clonazepam can be decreased when used in combination with Hyaluronidase. Clonidine The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Clonidine. Conjugated estrogens The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Conjugated estrogens. Corticotropin The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Corticotropin. Cortisone acetate The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Cortisone acetate. Cyclizine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Cyclizine. Dexamethasone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Dexamethasone. Dexamethasone acetate The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Dexamethasone acetate. Dexmedetomidine The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Dexmedetomidine. Diazepam The therapeutic efficacy of Diazepam can be decreased when used in combination with Hyaluronidase. Diethylstilbestrol The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Diethylstilbestrol. Dimenhydrinate The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Dimenhydrinate. Dimetindene The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Dimetindene. Dimetotiazine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Dimetotiazine. Diphenhydramine Hyaluronidase can cause an increase in the absorption of Diphenhydramine resulting in an increased serum concentration and potentially a worsening of adverse effects. Dobutamine The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Dobutamine. Dopamine The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Dopamine. Dyclonine Hyaluronidase can cause an increase in the absorption of Dyclonine resulting in an increased serum concentration and potentially a worsening of adverse effects. Emedastine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Emedastine. Ephedrine The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Ephedrine. Epinastine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Epinastine. Epinephrine The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Epinephrine. Ergometrine The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Ergometrine. Esterified estrogens The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Esterified estrogens. Estetrol The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Estetrol. Estradiol The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Estradiol. Estradiol acetate The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Estradiol acetate. Estradiol benzoate The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Estradiol benzoate. Estradiol cypionate The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Estradiol cypionate. Estradiol valerate The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Estradiol valerate. Estriol The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Estriol. Estrone sulfate The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Estrone sulfate. Ethinylestradiol The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Ethinylestradiol. Etidocaine Hyaluronidase can cause an increase in the absorption of Etidocaine resulting in an increased serum concentration and potentially a worsening of adverse effects. Etilefrine The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Etilefrine. Etomidate The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Etomidate. Famotidine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Famotidine. Fluocinolone acetonide The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Fluocinolone acetonide. Fluorometholone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Fluorometholone. Fluprednisolone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Fluprednisolone. Fosphenytoin The therapeutic efficacy of Fosphenytoin can be decreased when used in combination with Hyaluronidase. Furosemide The therapeutic efficacy of Furosemide can be decreased when used in combination with Hyaluronidase. Halazepam The therapeutic efficacy of Halazepam can be decreased when used in combination with Hyaluronidase. Hydrocortisone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Hydrocortisone. Hydrocortisone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Hydrocortisone succinate. Hydroxyzine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Hydroxyzine. Imipramine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Imipramine. Lidocaine Hyaluronidase can cause an increase in the absorption of Lidocaine resulting in an increased serum concentration and potentially a worsening of adverse effects. Lorazepam The therapeutic efficacy of Lorazepam can be decreased when used in combination with Hyaluronidase. Maprotiline The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Maprotiline. Meloxicam Hyaluronidase can cause an increase in the absorption of Meloxicam resulting in an increased serum concentration and potentially a worsening of adverse effects. Mephentermine The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Mephentermine. Mepivacaine Hyaluronidase can cause an increase in the absorption of Mepivacaine resulting in an increased serum concentration and potentially a worsening of adverse effects. Meprednisone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Meprednisone. Mestranol The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Mestranol. Metaraminol The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Metaraminol. Methantheline The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Methantheline. Methdilazine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Methdilazine. Methotrimeprazine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Methotrimeprazine. Methoxamine The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Methoxamine. Methyldopa The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Methyldopa. Methylprednisolone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Methylprednisolone. Methylprednisolone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Methylprednisolone hemisuccinate. Midazolam The therapeutic efficacy of Midazolam can be decreased when used in combination with Hyaluronidase. Mirtazapine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Mirtazapine. Nizatidine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Nizatidine. Norepinephrine The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Norepinephrine. Olanzapine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Olanzapine. Orphenadrine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Orphenadrine. Oxybuprocaine Hyaluronidase can cause an increase in the absorption of Oxybuprocaine resulting in an increased serum concentration and potentially a worsening of adverse effects. Oxymetazoline The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Oxymetazoline. Phenindamine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Phenindamine. Pheniramine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Pheniramine. Phenol Hyaluronidase can cause an increase in the absorption of Phenol resulting in an increased serum concentration and potentially a worsening of adverse effects. Phenyl aminosalicylate The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Phenyl aminosalicylate. Phenylephrine The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Phenylephrine. Phenytoin The therapeutic efficacy of Phenytoin can be decreased when used in combination with Hyaluronidase. Polyestradiol phosphate The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Polyestradiol phosphate. Prednisolone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Prednisolone. Prednisolone acetate The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Prednisolone acetate. Prednisone acetate The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Prednisone acetate. Prilocaine Hyaluronidase can cause an increase in the absorption of Prilocaine resulting in an increased serum concentration and potentially a worsening of adverse effects. Procaine Hyaluronidase can cause an increase in the absorption of Procaine resulting in an increased serum concentration and potentially a worsening of adverse effects. Promazine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Promazine. Promethazine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Promethazine. Proparacaine Hyaluronidase can cause an increase in the absorption of Proparacaine resulting in an increased serum concentration and potentially a worsening of adverse effects. Propiomazine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Propiomazine. Propoxycaine Hyaluronidase can cause an increase in the absorption of Propoxycaine resulting in an increased serum concentration and potentially a worsening of adverse effects. Quinestrol The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Quinestrol. Racepinephrine The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Racepinephrine. Ranitidine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Ranitidine. Remimazolam The therapeutic efficacy of Remimazolam can be decreased when used in combination with Hyaluronidase. Risperidone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Risperidone. Salicylic acid The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Salicylic acid. S Estrogens, A The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Synthetic Conjugated Estrogens, A. S Estrogens, B The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Synthetic Conjugated Estrogens, B. Tetracaine Hyaluronidase can cause an increase in the absorption of Tetracaine resulting in an increased serum concentration and potentially a worsening of adverse effects. Tetryzoline The risk or severity of adverse effects can be increased when Hyaluronidase is combined with Tetryzoline. Tibolone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Tibolone. Trazodone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Trazodone. Triamcinolone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Triamcinolone. Trilostane The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Trilostane. Tritoqualine The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Tritoqualine. Ziprasidone The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Ziprasidone. Zuclopenthixol The therapeutic efficacy of Hyaluronidase can be decreased when used in combination with Zuclopenthixol. Pregnancy and Lactation AU TGA pregnancy category: Exempt US FDA pregnancy category: Not assigned Pregnancy Medications exempted from pregnancy classification are not absolutely safe for use in pregnancy in all circumstances. Some exempted medicines, for example, the complementary medicine, St John's Wort, may interact with other medicines and induce unexpected adverse effects in the mother and/or fetus. Lactation Consider the developmental and health benefits of breastfeeding along with the mother's clinical need for this medication as well as any potential adverse effects from this drug or the underlying maternal condition. How should this medicine be used?

Daratumumab and hyaluronidase-fihj injection comes as a solution (liquid) to be injected subcutaneously (just under the skin) into the abdomen (stomach) over 3 to 5 minutes. The length of your treatment will depend on your condition and how well your body responds to treatment. A doctor or nurse will watch you closely while you are receiving the medication and afterwards to be sure you are not having a serious reaction to the medication. You will be given other medications to…

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Foodborne Illness (also foodborne disease and colloquially referred to as food poisoning)[rx] is any illness resulting from the spoilage of contaminated food, pathogenic bacteria, viruses, or parasites that…