Morphine
Yi palo
| Names | |
|---|---|
| Pronunciation | /ˈmɔːrfiːn/ |
| Trade names | Statex, MSContin, Oramorph, Sevredol, and others[1] |
| |
| Clinical data | |
| Drug class | Opioid |
| Main uses | Severe pain[2] |
| Side effects | Decreased respiratory effort, low blood pressure, abuse[3] |
| WHO AWaRe | Script error: No such module "WDfetch". |
| Dependence risk | High |
| Addiction risk | High[4] |
| Pregnancy category | Tɛmplet:Infobox drug/pregnancy category |
| Routes of use | Inhalation (smoking), insufflation (snorting), by mouth (PO), rectal, subcutaneous (SC), intramuscular (IM), intravenous (IV), epidural, and intrathecal (IT) |
| Onset of action | 5 minutes (IV), 15 minutes (IM),[5] 20 minutes (PO)[6] |
| Duration of action | 3–7 hours[3][7] |
| Defined daily dose | 100 mg (by mouth)[8] 30 mg (injection, rectal)[8] |
| Urine detection | 2 to 5 days[9] |
| External links | |
| AHFS/Drugs.com | Tɛmplet:Drugs.com |
| Legal | |
| [[Regulation of therapeutic goods |Tɛmplet:Engvar data]] | Tɛmplet:Infobox drug/licence |
| Legal status | Tɛmplet:Infobox drug/legal status |
| Pharmacokinetics | |
| Bioavailability | 20–40% (by mouth), 36–71% (rectally),[10] 100% (IV/IM) |
| Protein binding | 30–40% |
| Metabolism | Liver 90% |
| Elimination half-life | 2–3 hours |
| Excretion | Renal 90%, biliary 10% |
| Identifiers | |
| CAS Number | |
| PubChem CID | |
| PubChem SID | |
| IUPHAR/BPS | |
| DrugBank | |
| ChemSpider | |
| UNII | |
| KEGG | |
| ChEBI | |
| ChEMBL | |
| NIAID ChemDB | |
| PDB ligand | |
| CompTox Dashboard (EPA) | |
| ATC code | |
| Chemical and physical data | |
| Formula | Tɛmplet:Infobox drug/chemical formula |
| Molar mass | Tɛmplet:Chem molar mass |
| 3D model (JSmol) | |
| Solubility in water | HCl & sulf.: 60 mg/mL (20 °C) |
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Tɛmplet:Infobox drug/maintenance categories
Morphine nyɛla tila shɛli din tibiri biɛrim, ka bie opiate tilaa zuliya puuni , ka di tooi ka di bie tihi, binkɔbiri n ti pahi ninsali nima ni.[11][12]
References
[mali niŋ | mali mi di yibu sheena n-niŋ]- ↑ drugs.com Drugs.com international listings for Morphine Archived 14 Silimin gɔli June 2015 at the Wayback Machine Page accessed 2 June 2015
- ↑ MORPHINE injectable - Essential drugs. Archived 28 Silimin gɔli August 2021 at the Wayback Machine
- 1 2 Morphine sulfate. The American Society of Health-System Pharmacists. Archived 2 Silimin gɔli May 2015 at the Wayback Machine
- ↑ Bonewit-West, Kathy; Hunt, Sue A.; Applegate, Edith (2012). Today's Medical Assistant: Clinical and Administrative Procedures (in English). Elsevier Health Sciences. p. 571. ISBN 9781455701506. Archived from the original on 28 July 2020. Retrieved 2 August 2020. Archived 29 Silimin gɔli September 2024 at the Wayback Machine
- ↑ Whimster, Fiona (1997). Cambridge textbook of accident and emergency medicine. Cambridge: Cambridge University Press. p. 191. ISBN 978-0-521-43379-2. Archived from the original on 8 September 2017.
- ↑ Liben, Stephen (2012). Oxford textbook of palliative care for children (2 ed.). Oxford: Oxford University Press. p. 240. ISBN 978-0-19-959510-5. Archived from the original on 8 September 2017.
- ↑ Rockwood, Charles A. (2009). Rockwood and Wilkins' fractures in children (7th ed.). Philadelphia, Pa.: Lippincott Williams & Wilkins. p. 54. ISBN 978-1-58255-784-7. Archived from the original on 8 September 2017.
- 1 2 WHOCC - ATC/DDD Index. Archived 4 Silimin gɔli August 2020 at the Wayback Machine
- ↑ Interpreting Urine Drug Tests (UDT). Archived 25 Silimin gɔli October 2023 at the Wayback Machine
- ↑ (April 1988) "The bioavailability of rectally administered morphine". Pharmacology & Toxicology 62 (4): 203–5. DOI:10.1111/j.1600-0773.1988.tb01872.x. PMID 3387374.
- ↑ Morphine sulfate. The American Society of Health-System Pharmacists.
- ↑ (2012) "Endogenous morphine: up-to-date review 2011". Folia Biologica 58 (2): 49–56. PMID 22578954. “Positive evolutionary pressure has apparently preserved the ability to synthesize chemically authentic morphine, albeit in homeopathic concentrations, throughout animal phyla.”