The authors make no claims of the accuracy of the information contained
herein; and these suggested doses and/or guidelines are not a substitute for clinical judgment. Neither GlobalRPh Inc. nor any other party involved in the
preparation of this document shall be liable for any special,
consequential, or exemplary damages resulting in whole or part from any
user's use of or reliance upon this material. PLEASE
READ THE DISCLAIMER CAREFULLY BEFORE
ACCESSING OR USING THIS SITE. BY ACCESSING OR USING THIS SITE, YOU AGREE
TO BE BOUND BY THE TERMS AND CONDITIONS SET FORTH IN THE DISCLAIMER.
Usual Diluents
D5W, NS
Standard Dilutions [Amount of drug]
[Infusion volume] [Infusion rate]
Usual concentration for continuous I.V. infusion: 0.1 to 1 mg/mL in D5W.
Parenteral drug products should be inspected for particulate matter and
discoloration prior to administration, whenever solution and container
permit. DO NOT USE IF COLOR IS DARKER THAN PALE YELLOW, IF IT IS
DISCOLORED IN ANY OTHER WAY OR IF IT CONTAINS A PRECIPITATE.
Stability / Miscellaneous
Exp: 7 days (RT / REF).
Some studies indicate stability up to 30 days. Usual rate: 1 to 10
mg/hr.
DRUG ABUSE AND DEPENDENCE
Controlled Substance CII
Morphine sulfate is a Schedule II narcotic under the United States
Controlled Substance Act (21 U.S.C. 801-886). Morphine is the most
commonly cited prototype for narcotic substances that possess an
addiction-forming or addiction-sustaining liability. As with all potent
opioids which are µ-agonists, tolerance, psychological and physical
dependence to morphine may develop. Individuals with a prior history of
opioid or other substance abuse or dependence would be considered to be
at greater risk. Care must be taken to avert withdrawal in patients who
have been maintained on parenteral/oral narcotics. Withdrawal symptoms
may occur when morphine is discontinued abruptly or upon administration
of a narcotic antagonist.
Withdrawal symptoms in patients dependent on morphine begin shortly
before the time of the next scheduled dose, reach a peak at 36 to 72
hours after the last dose, and then slowly subside over a period of 7
to 10 days. Symptoms include yawning, sweating, lacrimation. rhinorrhea,
a restless, tossing sleep, dilated pupils, gooseflesh, irritability,
tremor, nausea, vomiting, and diarrhea.
Treatment of the abstinence syndrome is primarily symptomatic and
supportive, including maintenance of proper fluid and electrolyte
balance.
OVERDOSAGE
Overdosage of morphine is characterized by respiratory depression, with
or without concomitant CNS depression. Mild overdosage may be managed
by continuous stimulation of the patient and/or frequent verbal
instructions to "Wake-up" or "Take a deep breath". Serious overdose
with morphine is characterized by profound respiratory depression (a
decrease in respiratory rate/or tidal volume, Cheyne-Stokes
respiration, cyanosis), extreme somnolence progressing to stupor or
coma, skeletal muscle flaccidity, cold and clammy skin, and sometimes
bradycardia and hypotension. The triad of coma, pinpoint pupils and
respiratory depression is strongly suggestive of opiate poisoning.
Primary attention should be given to the establishment of adequate
respiratory exchange through maintenance of a patent airway and
institution of assisted, or controlled, ventilation. The narcotic
antagonist, naloxone, is a specific antidote. An initial dose of 0.4 to
2 mg of naloxone should be administered intravenously, simultaneously
with respiratory resuscitation. If the desired degree of counteraction
and improvement in respiratory function is not obtained, naloxone may
be repeated at 2 to 3 minute intervals. If no response is observed
after 10 mg of naloxone has been administered, the diagnosis of
morphine-induced toxicity should be questioned. Intramuscular or
subcutaneous administration of naloxone may be used if the intravenous
route is not available. As the duration of effect of naloxone is
considerably shorter than that of morphine, repeated administration may
be necessary.
The authors make no claims of the accuracy of the information contained herein; and these suggested doses are not a substitute for clinical
judgment. Neither GlobalRPh Inc. nor any other party involved in the
preparation of this program shall be liable for any special, consequential, or exemplary damages resulting in whole or part from any user's use of or reliance upon this material. PLEASE READ THE DISCLAIMER
CAREFULLY
BEFORE ACCESSING OR USING THIS SITE. BY ACCESSING OR USING THIS SITE, YOU
AGREE TO BE BOUND BY THE TERMS AND CONDITIONS SET FORTH IN THE DISCLAIMER.