AIDS ANTIVIRAL CCR5 RECEPTOR ANTAGONISTS
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
Antiviral CCR5 receptor antagonists, AIDS CCR5 receptor antagonists HIV, AIDS antiviral CCR5 receptor antagonists UK 427857 CAS 376348-65-1 SCH 417690 Schering D
Antiviral CCR5 receptor antagonists, AIDS CCR5 receptor antagonists HIV, AIDS antiviral CCR5 receptor antagonists
IDENTIFIERS
USES/FORMS/SOURCES
Maraviroc is FDA-approved as treatment, in combination with other antiretroviral agents, in treatment-experienced adults infected with only CCR5-tropic HIV-1 detectable strain and who have evidence of viral replication and HIV-1 strains that are resistant to multiple antiretroviral agents (Prod Info SELZENTRY(R) oral tablets, 2007). At the time of this review, vicriviroc is an investigational CCR5 inhibitor undergoing phase II clinical trials (Gulick et al, 2007).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- USES: Maraviroc, a CCR5 receptor antagonist, is used in combination with other antiretroviral agents in the treatment of adults infected with CCR5-tropic HIV-1 virus.
- PHARMACOLOGY: Maraviroc is a chemokine receptor antagonist that prevents HIV infection of CD4 T-cells by blocking the CCR5 receptor. Specifically, maraviroc prevents the membrane fusion events necessary for viral entry by blocking the binding of viral envelope, glycoprotein (gp) 120, to CCR5. Maraviroc is inactive against isolates that utilize CXCR4 as a co-receptor; therefore, the antiviral mechanism of action of maraviroc is exclusively CCR5-mediated.
- EPIDEMIOLOGY: Overdose is rare.
COMMON: The most common adverse effects following therapeutic administration of maraviroc, occurring at an incidence greater than 8%, include cough, pyrexia, upper respiratory tract infections, rash, abdominal pain, and dizziness. The dose-limiting toxicity, observed following oral administration of 600 mg, is postural hypotension. INFREQUENT: Other adverse effects that have occurred less frequently include myocardial infarction, myocardial ischemia, pruritus, constipation, hepatotoxicity, including elevated liver enzymes and hepatitis, myalgia, arthralgia, paresthesias and dysesthesias, and insomnia. DOSE-LIMITING: The dose-limiting toxicity, observed following oral administration of 600 mg maraviroc, is postural hypotension.
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
-FIRST AID
FIRST AID AND PREHOSPITAL TREATMENT
Consider activated charcoal if the overdose is recent, the patient is not vomiting, and is able to maintain airway. PREHOSPITAL ACTIVATED CHARCOAL ADMINISTRATION Consider prehospital administration of activated charcoal as an aqueous slurry in patients with a potentially toxic ingestion who are awake and able to protect their airway. Activated charcoal is most effective when administered within one hour of ingestion. Administration in the prehospital setting has the potential to significantly decrease the time from toxin ingestion to activated charcoal administration, although it has not been shown to affect outcome (Alaspaa et al, 2005; Thakore & Murphy, 2002; Spiller & Rogers, 2002). In patients who are at risk for the abrupt onset of seizures or mental status depression, activated charcoal should not be administered in the prehospital setting, due to the risk of aspiration in the event of spontaneous emesis. The addition of flavoring agents (cola drinks, chocolate milk, cherry syrup) to activated charcoal improves the palatability for children and may facilitate successful administration (Guenther Skokan et al, 2001; Dagnone et al, 2002).
CHARCOAL DOSE Use a minimum of 240 milliliters of water per 30 grams charcoal (FDA, 1985). Optimum dose not established; usual dose is 25 to 100 grams in adults and adolescents; 25 to 50 grams in children aged 1 to 12 years (or 0.5 to 1 gram/kilogram body weight) ; and 0.5 to 1 gram/kilogram in infants up to 1 year old (Chyka et al, 2005). Routine use of a cathartic with activated charcoal is NOT recommended as there is no evidence that cathartics reduce drug absorption and cathartics are known to cause adverse effects such as nausea, vomiting, abdominal cramps, electrolyte imbalances and occasionally hypotension (None Listed, 2004).
ADVERSE EFFECTS/CONTRAINDICATIONS Complications: emesis, aspiration (Chyka et al, 2005). Aspiration may be complicated by acute respiratory failure, ARDS, bronchiolitis obliterans or chronic lung disease (Golej et al, 2001; Graff et al, 2002; Pollack et al, 1981; Harris & Filandrinos, 1993; Elliot et al, 1989; Rau et al, 1988; Golej et al, 2001; Graff et al, 2002). Refer to the ACTIVATED CHARCOAL/TREATMENT management for further information. Contraindications: unprotected airway (increases risk/severity of aspiration) , nonfunctioning gastrointestinal tract, uncontrolled vomiting, and ingestion of most hydrocarbons (Chyka et al, 2005).
-RANGE OF TOXICITY
MAXIMUM TOLERATED EXPOSURE
- MARAVIROC: A specific toxic dose has not been established. Postural hypotension was observed following oral administration of 600 mg during clinical trials, and is reported to be the dose-limiting toxicity. Doses up to 1200 mg have been used in clinical trials (Prod Info SELZENTRY(R) oral tablets, 2013).
- Carcinogenicity Ratings for CAS376348-65-1 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed EPA (U.S. Environmental Protection Agency, 2011): Not Listed IARC (International Agency for Research on Cancer (IARC), 2016; International Agency for Research on Cancer, 2015; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010a; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2008; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2007; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2006; IARC, 2004): Not Listed NIOSH (National Institute for Occupational Safety and Health, 2007): Not Listed MAK (DFG, 2002): Not Listed NTP (U.S. Department of Health and Human Services, Public Health Service, National Toxicology Project ): Not Listed
TOXICITY AND RISK ASSESSMENT VALUES
- EPA Risk Assessment Values for CAS376348-65-1 (U.S. Environmental Protection Agency, 2011):
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS376348-65-1 (American Conference of Governmental Industrial Hygienists, 2010):
- AIHA WEEL Values for CAS376348-65-1 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS376348-65-1 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS376348-65-1 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS376348-65-1 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS376348-65-1 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS376348-65-1 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS376348-65-1 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS376348-65-1 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS376348-65-1 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS376348-65-1 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS376348-65-1 (EPA, 2005):
LABELS
- NFPA Hazard Ratings for CAS376348-65-1 (NFPA, 2002):
-PERSONAL PROTECTION
SUMMARY
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 376348-65-1.
-PHYSICAL HAZARDS
FIRE HAZARD
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS376348-65-1 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
- NFPA Extinguishing Methods for CAS376348-65-1 (NFPA, 2002):
EVACUATION PROCEDURES
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
- AIHA ERPG Values for CAS376348-65-1 (AIHA, 2006):
- DOE TEEL Values for CAS376348-65-1 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS376348-65-1 (National Research Council, 2010; National Research Council, 2009; National Research Council, 2008; National Research Council, 2007; NRC, 2001; NRC, 2002; NRC, 2003; NRC, 2004; NRC, 2004; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; 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62 FR 58840, 1997; 65 FR 14186, 2000; 65 FR 39264, 2000; 65 FR 77866, 2000; 66 FR 21940, 2001; 67 FR 7164, 2002; 68 FR 42710, 2003; 69 FR 54144, 2004):
- NIOSH IDLH Values for CAS376348-65-1 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
- MARAVIROC - 513.67 (Prod Info SELZENTRY(R) oral tablets, 2007)
DESCRIPTION/PHYSICAL STATE
- Maraviroc is a white to pale-colored powder and is highly soluble across the physiological pH range (pH 1 to 7.5) (Prod Info SELZENTRY(R) oral tablets, 2007).
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