Treatment algorithm
Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups: see disclaimer
foodborne botulism
supportive care
Supportive care is the mainstay of botulism therapy.[41]Rao AK, Sobel J, Chatham-Stephens K, et al. Clinical Guidelines for Diagnosis and Treatment of Botulism, 2021. MMWR Recomm Rep. 2021 May 7;70(2):1-30. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112830 http://www.ncbi.nlm.nih.gov/pubmed/33956777?tool=bestpractice.com
Patients with suspected or confirmed botulism should undergo serial vital capacity assessments in the intensive care unit.
In addition, patients should be assessed for the adequacy of gag and cough reflexes, control of oropharyngeal secretions, oxygen saturation, and inspiratory force.
Mechanical ventilation should be considered for any patient with upper airway compromise (due to pharyngeal muscle paralysis) or a decline in vital capacity.
botulism antitoxin
Treatment recommended for ALL patients in selected patient group
Swift administration of antitoxin is essential.[41]Rao AK, Sobel J, Chatham-Stephens K, et al. Clinical Guidelines for Diagnosis and Treatment of Botulism, 2021. MMWR Recomm Rep. 2021 May 7;70(2):1-30. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112830 http://www.ncbi.nlm.nih.gov/pubmed/33956777?tool=bestpractice.com
Toxin types A, B, and E account for most cases of foodborne botulism.
In March 2013 the Food and Drug Administration approved the use of the heptavalent botulism antitoxin (HBAT).
HBAT, available only through the Centers for Disease Control and Prevention (CDC), replaces previously licensed botulism antitoxin AB and investigational botulism antitoxin E.[63]Centers for Disease Control and Prevention (CDC). Investigational heptavalent botulinum antitoxin (HBAT) to replace licensed botulinum antitoxin AB and investigational botulinum antitoxin E. MMWR Morb Mortal Wkly Rep. 2010 Mar 19;59(10):299. http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5910a4.htm http://www.ncbi.nlm.nih.gov/pubmed/20300057?tool=bestpractice.com The potential for anaphylaxis, delayed allergic reactions (serum sickness), and lifelong sensitization to equine proteins, in addition to short half-lives, limits the use of antitoxins derived from equine plasma (such as HBAT) in the infant (<1 year) population.[64]Arnon SS, Schechter R, Maslanka SE, et al. Human botulism immune globulin for the treatment of infant botulism. N Engl J Med. 2006 Feb 2;354(5):462-71. http://www.nejm.org/doi/full/10.1056/NEJMoa051926#t=article http://www.ncbi.nlm.nih.gov/pubmed/16452558?tool=bestpractice.com
A dose of HBAT contains equine-derived antibody to 7 botulinum toxin types (A-G) with a minimum potency of 4500 units of serotype A antitoxin, 3300 units of serotype B antitoxin, 3000 units of serotype C antitoxin, 600 units of serotype D antitoxin, 5100 units of serotype E antitoxin, 3000 units of serotype F antitoxin, and 600 units of serotype G antitoxin.
CDC contact number in US: 770-488-7100 (24-hour line).
Primary options
botulism antitoxin heptavalent (equine): consult specialist for guidance on dose
gastric lavage or enemas
Treatment recommended for SOME patients in selected patient group
Gastric lavage may be attempted if the food exposure was relatively recent.
In the absence of an ileus, enemas may be used to eliminate unabsorbed toxin from the gastrointestinal tract.
supportive care
Supportive care is the mainstay of botulism therapy.[41]Rao AK, Sobel J, Chatham-Stephens K, et al. Clinical Guidelines for Diagnosis and Treatment of Botulism, 2021. MMWR Recomm Rep. 2021 May 7;70(2):1-30. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112830 http://www.ncbi.nlm.nih.gov/pubmed/33956777?tool=bestpractice.com
Respiratory status must be monitored closely through frequent monitoring of patient’s respiratory rate, pulse oximetry, and arterial blood gases, as needed.
In addition, patients should be assessed for the adequacy of gag and cough reflexes, control of oropharyngeal secretions, oxygen saturation, and inspiratory force.
Mechanical ventilation should be considered for any patient with upper airway compromise (due to pharyngeal muscle paralysis) or a decline in vital capacity.
botulism immunoglobulin
Treatment recommended for ALL patients in selected patient group
Swift administration of intravenous botulism immunoglobulin (human), also known as BabyBIG™, is essential in infants <1 year of age with botulism type A or B.
It has been shown to be safe and effective for the treatment of infected infants in a randomized, controlled trial. Treatment was associated with reduction in the mean length of hospital stay, duration of mechanical ventilation, and associated costs when compared with treatment with intravenous immunoglobulin.[64]Arnon SS, Schechter R, Maslanka SE, et al. Human botulism immune globulin for the treatment of infant botulism. N Engl J Med. 2006 Feb 2;354(5):462-71. http://www.nejm.org/doi/full/10.1056/NEJMoa051926#t=article http://www.ncbi.nlm.nih.gov/pubmed/16452558?tool=bestpractice.com [65]Chalk CH, Benstead TJ, Pound JD, et al. Medical treatment for botulism. Cochrane Database Syst Rev. 2019 Apr 17;(4):CD008123. https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD008123.pub4/full http://www.ncbi.nlm.nih.gov/pubmed/30993666?tool=bestpractice.com
A single dose is used in suspected or confirmed cases. Its half-life is 28 days.
Information and supply is from the California Department of Health Services. Infant Botulism Treatment and Prevention Program Opens in new window
Human-derived botulism immunoglobulin is preferred in the infant (<1 year) population because antitoxins derived from equine plasma (such as heptavalent botulism antitoxin) have shorter half-lives, and have been associated with anaphylaxis, delayed allergic reactions (serum sickness), and lifelong sensitization to equine proteins.[64]Arnon SS, Schechter R, Maslanka SE, et al. Human botulism immune globulin for the treatment of infant botulism. N Engl J Med. 2006 Feb 2;354(5):462-71. http://www.nejm.org/doi/full/10.1056/NEJMoa051926#t=article http://www.ncbi.nlm.nih.gov/pubmed/16452558?tool=bestpractice.com
Primary options
botulism immune globulin (human): dose may vary with each manufactured lot; consult specialist for guidance on dose
wound botulism
supportive care
Supportive care is the mainstay of botulism therapy.[41]Rao AK, Sobel J, Chatham-Stephens K, et al. Clinical Guidelines for Diagnosis and Treatment of Botulism, 2021. MMWR Recomm Rep. 2021 May 7;70(2):1-30. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112830 http://www.ncbi.nlm.nih.gov/pubmed/33956777?tool=bestpractice.com
Patients with suspected or confirmed botulism should undergo serial vital capacity assessments in the intensive care unit.
In addition, patients should be assessed for the adequacy of gag and cough reflexes, control of oropharyngeal secretions, oxygen saturation, and inspiratory force.
Mechanical ventilation should be considered for any patient with upper airway compromise (due to pharyngeal muscle paralysis) or a decline in vital capacity.
botulism antitoxin
Treatment recommended for ALL patients in selected patient group
Swift administration of antitoxin is essential.[41]Rao AK, Sobel J, Chatham-Stephens K, et al. Clinical Guidelines for Diagnosis and Treatment of Botulism, 2021. MMWR Recomm Rep. 2021 May 7;70(2):1-30. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112830 http://www.ncbi.nlm.nih.gov/pubmed/33956777?tool=bestpractice.com
In March 2013 the Food and Drug Administration approved the use of the heptavalent botulism antitoxin (HBAT).
HBAT, available only through the Centers for Disease Control and Prevention (CDC), replaces previously licensed botulism antitoxin AB and investigational botulism antitoxin E.[63]Centers for Disease Control and Prevention (CDC). Investigational heptavalent botulinum antitoxin (HBAT) to replace licensed botulinum antitoxin AB and investigational botulinum antitoxin E. MMWR Morb Mortal Wkly Rep. 2010 Mar 19;59(10):299. http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5910a4.htm http://www.ncbi.nlm.nih.gov/pubmed/20300057?tool=bestpractice.com The potential for anaphylaxis, delayed allergic reactions (serum sickness), and lifelong sensitization to equine proteins, in addition to short half-lives, limits the use of antitoxins derived from equine plasma (such as HBAT) in the infant (<1 year) population.[64]Arnon SS, Schechter R, Maslanka SE, et al. Human botulism immune globulin for the treatment of infant botulism. N Engl J Med. 2006 Feb 2;354(5):462-71. http://www.nejm.org/doi/full/10.1056/NEJMoa051926#t=article http://www.ncbi.nlm.nih.gov/pubmed/16452558?tool=bestpractice.com
A dose of HBAT contains equine-derived antibody to 7 botulinum toxin types (A-G) with a minimum potency of 4500 units of serotype A antitoxin, 3300 units of serotype B antitoxin, 3000 units of serotype C antitoxin, 600 units of serotype D antitoxin, 5100 units of serotype E antitoxin, 3000 units of serotype F antitoxin, and 600 units of serotype G antitoxin.
CDC contact number in US: 770-488-7100 (24-hour line).
Primary options
botulism antitoxin heptavalent (equine): consult specialist for guidance on dose
debridement and antibiotics
Treatment recommended for ALL patients in selected patient group
Patients with wound botulism should undergo careful debridement.
Clostridium botulinum abscess formation may be treated with penicillin G, or metronidazole in penicillin-allergic patients. Aminoglycosides should be avoided in cases of confirmed or suspected botulism as they have been shown to cause neuromuscular blockade, and may therefore potentiate the toxin's effects.[66]Santos JI, Swensen P, Glasgow LA. Potentiation of Clostridium botulinum toxin aminoglycoside antibiotics: clinical and laboratory observations. Pediatrics. 1981 Jul;68(1):50-4. http://www.ncbi.nlm.nih.gov/pubmed/7243509?tool=bestpractice.com
Primary options
debridement
and
penicillin G potassium: children: consult specialist for guidance on dose; adults: 10-20 million units/day intravenously given in divided doses every 4-6 hours
Secondary options
debridement
and
metronidazole: children: consult specialist for guidance on dose; adults: 500 mg intravenously every 8 hours
supportive care
Supportive care is the mainstay of botulism therapy.[41]Rao AK, Sobel J, Chatham-Stephens K, et al. Clinical Guidelines for Diagnosis and Treatment of Botulism, 2021. MMWR Recomm Rep. 2021 May 7;70(2):1-30. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112830 http://www.ncbi.nlm.nih.gov/pubmed/33956777?tool=bestpractice.com
Respiratory status must be monitored closely through frequent monitoring of patient’s respiratory rate, pulse oximetry, and arterial blood gases, as needed.
In addition, patients should be assessed for the adequacy of gag and cough reflexes, control of oropharyngeal secretions, oxygen saturation, and inspiratory force.
Mechanical ventilation should be considered for any patient with upper airway compromise (due to pharyngeal muscle paralysis) or a decline in vital capacity.
botulism immunoglobulin
Treatment recommended for ALL patients in selected patient group
Swift administration of intravenous botulism immunoglobulin (human), also known as BabyBIG™, is essential in infants <1 year of age with botulism type A or B.
It has been shown to be safe and effective for the treatment of infected infants in a randomized, controlled trial. Treatment was associated with reduction in the mean length of hospital stay, duration of mechanical ventilation, and associated costs when compared with treatment with intravenous immunoglobulin.[64]Arnon SS, Schechter R, Maslanka SE, et al. Human botulism immune globulin for the treatment of infant botulism. N Engl J Med. 2006 Feb 2;354(5):462-71. http://www.nejm.org/doi/full/10.1056/NEJMoa051926#t=article http://www.ncbi.nlm.nih.gov/pubmed/16452558?tool=bestpractice.com [65]Chalk CH, Benstead TJ, Pound JD, et al. Medical treatment for botulism. Cochrane Database Syst Rev. 2019 Apr 17;(4):CD008123. https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD008123.pub4/full http://www.ncbi.nlm.nih.gov/pubmed/30993666?tool=bestpractice.com
A single dose is used in suspected or confirmed cases. Its half-life is 28 days.
Information and supply is from the California Department of Health Services. Infant Botulism Treatment and Prevention Program Opens in new window
Human-derived botulism immunoglobulin is preferred in the infant (<1 year) population because antitoxins derived from equine plasma (such as heptavalent botulism antitoxin) have shorter half-lives, and have been associated with anaphylaxis, delayed allergic reactions (serum sickness), and lifelong sensitization to equine proteins.[64]Arnon SS, Schechter R, Maslanka SE, et al. Human botulism immune globulin for the treatment of infant botulism. N Engl J Med. 2006 Feb 2;354(5):462-71. http://www.nejm.org/doi/full/10.1056/NEJMoa051926#t=article http://www.ncbi.nlm.nih.gov/pubmed/16452558?tool=bestpractice.com
Primary options
botulism immune globulin (human): dose may vary with each manufactured lot; consult specialist for guidance on dose
debridement and antibiotics
Treatment recommended for ALL patients in selected patient group
Patients with wound botulism should undergo careful debridement.
Clostridium botulinum abscess formation may be treated with penicillin G, or metronidazole in penicillin-allergic patients. Aminoglycosides should be avoided in cases of confirmed or suspected botulism as they have been shown to cause neuromuscular blockade, and may therefore potentiate the toxin's effects.[66]Santos JI, Swensen P, Glasgow LA. Potentiation of Clostridium botulinum toxin aminoglycoside antibiotics: clinical and laboratory observations. Pediatrics. 1981 Jul;68(1):50-4. http://www.ncbi.nlm.nih.gov/pubmed/7243509?tool=bestpractice.com
Primary options
debridement
and
penicillin G potassium: children: consult specialist for guidance on dose
Secondary options
debridement
and
metronidazole: children: consult specialist for guidance on dose
iatrogenic botulism
supportive care
Supportive care is the mainstay of botulism therapy.[41]Rao AK, Sobel J, Chatham-Stephens K, et al. Clinical Guidelines for Diagnosis and Treatment of Botulism, 2021. MMWR Recomm Rep. 2021 May 7;70(2):1-30. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112830 http://www.ncbi.nlm.nih.gov/pubmed/33956777?tool=bestpractice.com
Patients with suspected or confirmed botulism should undergo serial vital capacity assessments in the intensive care unit.
In addition, patients should be assessed for the adequacy of gag and cough reflexes, control of oropharyngeal secretions, oxygen saturation, and inspiratory force.
Mechanical ventilation should be considered for any patient with upper airway compromise (due to pharyngeal muscle paralysis) or a decline in vital capacity.
botulism antitoxin
Treatment recommended for ALL patients in selected patient group
Swift administration of antitoxin is essential.[41]Rao AK, Sobel J, Chatham-Stephens K, et al. Clinical Guidelines for Diagnosis and Treatment of Botulism, 2021. MMWR Recomm Rep. 2021 May 7;70(2):1-30. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112830 http://www.ncbi.nlm.nih.gov/pubmed/33956777?tool=bestpractice.com
In March 2013 the Food and Drug Administration approved the use of the heptavalent botulism antitoxin (HBAT).
HBAT, available only through the Centers for Disease Control and Prevention (CDC), replaces previously licensed botulism antitoxin AB and investigational botulism antitoxin E.[63]Centers for Disease Control and Prevention (CDC). Investigational heptavalent botulinum antitoxin (HBAT) to replace licensed botulinum antitoxin AB and investigational botulinum antitoxin E. MMWR Morb Mortal Wkly Rep. 2010 Mar 19;59(10):299. http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5910a4.htm http://www.ncbi.nlm.nih.gov/pubmed/20300057?tool=bestpractice.com The potential for anaphylaxis, delayed allergic reactions (serum sickness), and lifelong sensitization to equine proteins, in addition to short half-lives, limits the use of antitoxins derived from equine plasma (such as HBAT) in the infant (<1 year) population.[64]Arnon SS, Schechter R, Maslanka SE, et al. Human botulism immune globulin for the treatment of infant botulism. N Engl J Med. 2006 Feb 2;354(5):462-71. http://www.nejm.org/doi/full/10.1056/NEJMoa051926#t=article http://www.ncbi.nlm.nih.gov/pubmed/16452558?tool=bestpractice.com
A dose of HBAT contains equine-derived antibody to 7 botulinum toxin types (A-G) with a minimum potency of 4500 units of serotype A antitoxin, 3300 units of serotype B antitoxin, 3000 units of serotype C antitoxin, 600 units of serotype D antitoxin, 5100 units of serotype E antitoxin, 3000 units of serotype F antitoxin, and 600 units of serotype G antitoxin.
CDC contact number in US: 770-488-7100 (24-hour line).
Primary options
botulism antitoxin heptavalent (equine): consult specialist for guidance on dose
supportive care
Supportive care is the mainstay of botulism therapy.[41]Rao AK, Sobel J, Chatham-Stephens K, et al. Clinical Guidelines for Diagnosis and Treatment of Botulism, 2021. MMWR Recomm Rep. 2021 May 7;70(2):1-30. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112830 http://www.ncbi.nlm.nih.gov/pubmed/33956777?tool=bestpractice.com
Respiratory status must be monitored closely through frequent monitoring of patient’s respiratory rate, pulse oximetry, and arterial blood gases, as needed.
In addition, patients should be assessed for the adequacy of gag and cough reflexes, control of oropharyngeal secretions, oxygen saturation, and inspiratory force.
Mechanical ventilation should be considered for any patient with upper airway compromise (due to pharyngeal muscle paralysis) or a decline in vital capacity.
botulism immunoglobulin
Treatment recommended for ALL patients in selected patient group
Swift administration of intravenous botulism immunoglobulin (human), also known as BabyBIG™, is essential in infants <1 year of age with botulism type A or B.
It has been shown to be safe and effective for the treatment of infected infants in a randomized, controlled trial. Treatment was associated with reduction in the mean length of hospital stay, duration of mechanical ventilation, and associated costs when compared with treatment with intravenous immunoglobulin.[64]Arnon SS, Schechter R, Maslanka SE, et al. Human botulism immune globulin for the treatment of infant botulism. N Engl J Med. 2006 Feb 2;354(5):462-71. http://www.nejm.org/doi/full/10.1056/NEJMoa051926#t=article http://www.ncbi.nlm.nih.gov/pubmed/16452558?tool=bestpractice.com [65]Chalk CH, Benstead TJ, Pound JD, et al. Medical treatment for botulism. Cochrane Database Syst Rev. 2019 Apr 17;(4):CD008123. https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD008123.pub4/full http://www.ncbi.nlm.nih.gov/pubmed/30993666?tool=bestpractice.com
A single dose is used in suspected or confirmed cases. Its half-life is 28 days.
Information and supply is from the California Department of Health Services. Infant Botulism Treatment and Prevention Program Opens in new window
Human-derived botulism immunoglobulin is preferred in the infant (<1 year) population because antitoxins derived from equine plasma (such as heptavalent botulism antitoxin) have shorter half-lives, and have been associated with anaphylaxis, delayed allergic reactions (serum sickness), and lifelong sensitization to equine proteins.[64]Arnon SS, Schechter R, Maslanka SE, et al. Human botulism immune globulin for the treatment of infant botulism. N Engl J Med. 2006 Feb 2;354(5):462-71. http://www.nejm.org/doi/full/10.1056/NEJMoa051926#t=article http://www.ncbi.nlm.nih.gov/pubmed/16452558?tool=bestpractice.com
Primary options
botulism immune globulin (human): dose may vary with each manufactured lot; consult specialist for guidance on dose
inhalational botulism (biological attack)
supportive care and decontamination
Supportive care is the mainstay of botulism therapy.[41]Rao AK, Sobel J, Chatham-Stephens K, et al. Clinical Guidelines for Diagnosis and Treatment of Botulism, 2021. MMWR Recomm Rep. 2021 May 7;70(2):1-30. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112830 http://www.ncbi.nlm.nih.gov/pubmed/33956777?tool=bestpractice.com
Adults and children with suspected or confirmed botulism should undergo serial vital capacity assessments in the intensive care unit. In addition, patients should be assessed for the adequacy of gag and cough reflexes, control of oropharyngeal secretions, oxygen saturation, and inspiratory force.
Mechanical ventilation should be considered for any patient with upper airway compromise (due to pharyngeal muscle paralysis) or a decline in vital capacity.
Clothing and skin exposed to aerosolized botulinum toxin should be washed thoroughly with soap and water. As hours to days are required for natural degradation of the toxin, a 0.1% hypochlorite bleach solution should be used to clean exposed objects and surfaces.[47]Arnon SS, Schechter R, Inglesby TV, et al. Botulinum toxin as a biological weapon: medical and public health management. JAMA. 2001 Feb 28;285(8):1059-70. http://www.ncbi.nlm.nih.gov/pubmed/11209178?tool=bestpractice.com
botulism antitoxin or botulism immunoglobulin
Treatment recommended for ALL patients in selected patient group
Swift administration of heptavalent antitoxin is essential.[41]Rao AK, Sobel J, Chatham-Stephens K, et al. Clinical Guidelines for Diagnosis and Treatment of Botulism, 2021. MMWR Recomm Rep. 2021 May 7;70(2):1-30. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112830 http://www.ncbi.nlm.nih.gov/pubmed/33956777?tool=bestpractice.com
In the event of intentional dissemination of botulinum toxin, heptavalent antitoxin may be dispensed by the Department of Defense.[47]Arnon SS, Schechter R, Inglesby TV, et al. Botulinum toxin as a biological weapon: medical and public health management. JAMA. 2001 Feb 28;285(8):1059-70. http://www.ncbi.nlm.nih.gov/pubmed/11209178?tool=bestpractice.com
Botulism immunoglobulin (BabyBIG™) has not been tested in adults or children >1 year.
Primary options
botulism antitoxin heptavalent (equine): consult specialist for guidance on dose
Secondary options
botulism immune globulin (human): dose may vary with each manufactured lot; consult specialist for guidance on dose
supportive care and decontamination
Supportive care is the mainstay of botulism therapy.[41]Rao AK, Sobel J, Chatham-Stephens K, et al. Clinical Guidelines for Diagnosis and Treatment of Botulism, 2021. MMWR Recomm Rep. 2021 May 7;70(2):1-30. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112830 http://www.ncbi.nlm.nih.gov/pubmed/33956777?tool=bestpractice.com
Respiratory status must be monitored closely through frequent monitoring of patient’s respiratory rate, pulse oximetry, and arterial blood gases, as needed.
In addition, patients should be assessed for the adequacy of gag and cough reflexes, control of oropharyngeal secretions, oxygen saturation, and inspiratory force. Mechanical ventilation should be considered for any patient with upper airway compromise (due to pharyngeal muscle paralysis) or a decline in vital capacity.
Clothing and skin exposed to aerosolized botulinum toxin should be washed thoroughly with soap and water. As hours to days are required for natural degradation of the toxin, a 0.1% hypochlorite bleach solution should be used to clean exposed objects and surfaces.[47]Arnon SS, Schechter R, Inglesby TV, et al. Botulinum toxin as a biological weapon: medical and public health management. JAMA. 2001 Feb 28;285(8):1059-70. http://www.ncbi.nlm.nih.gov/pubmed/11209178?tool=bestpractice.com
botulism immunoglobulin
Treatment recommended for ALL patients in selected patient group
Swift administration of intravenous botulism immunoglobulin (human), also known as BabyBIG™, is essential in infants <1 year of age with botulism type A or B.
It has been shown to be safe and effective for the treatment of infected infants in a randomized, controlled trial. Treatment was associated with reduction in the mean length of hospital stay, duration of mechanical ventilation, and associated costs when compared with treatment with intravenous immunoglobulin.[64]Arnon SS, Schechter R, Maslanka SE, et al. Human botulism immune globulin for the treatment of infant botulism. N Engl J Med. 2006 Feb 2;354(5):462-71. http://www.nejm.org/doi/full/10.1056/NEJMoa051926#t=article http://www.ncbi.nlm.nih.gov/pubmed/16452558?tool=bestpractice.com [65]Chalk CH, Benstead TJ, Pound JD, et al. Medical treatment for botulism. Cochrane Database Syst Rev. 2019 Apr 17;(4):CD008123. https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD008123.pub4/full http://www.ncbi.nlm.nih.gov/pubmed/30993666?tool=bestpractice.com
A single dose is used in suspected or confirmed cases. Its half-life is 28 days.
Information and supply is from the California Department of Health Services. Infant Botulism Treatment and Prevention Program Opens in new window
Primary options
botulism immune globulin (human): dose may vary with each manufactured lot; consult specialist for guidance on dose
Choose a patient group to see our recommendations
Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups. See disclaimer
Use of this content is subject to our disclaimer