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26 Cards in this Set

  • Front
  • Back
DRUG CLASS- antidote, tocolytic, fat soluble vitamins
MAG SULFATE
OB USE- PREVENTION AND TREAMENT OF hypoprothrombonemia
prevention of hemorraghic disease of the newborn
MAG SULFATE
Dosage and route of administration- PO,SUBQ, IM, IV,
2.5-10MG, 1-2 MG INFANTS
mag sulfate
contrainidcations- hypersensitivity, use cautiously in impaired liver function
mag sulfate
SIDE EFFECTS- Muscle weakness.
Lack of energy and drowsiness.
Decreased effort in breathing (respiratory depression).
Low blood pressure and fast pulse.
These side effects can decrease over the duration of treatment and go away when the medication is stopped.
MAG SULFATE
Nursing implications- monitor for frank and occult bleeding, apply pressure to all venipuncture sites for at least 5min, PT should be monitored prior to threapy and throughout to monitor.
Parenteral rout e preferredbc of severe sensitivity, antidote for warfarin but not heparin
IF IV administration is unavoidable, push at 1MG/MIN
MAG SULFATE
medications used to suppress premature labor
Tocolytics
β2-adrenergic receptor agonist, used as a fast-acting bronchodilator (often used as a short-term asthma treatment) and as a tocolytic to delay premature labour.
terbutaline
Maternal - tachycardia, nervousness, tremors, headache, hyperglycemia, hypokalemia, and rarely, pulmonary edema.[1]
Fetal - tachycardia and hypoglycemia
terbutaline side effects
orally (by mouth), by injection under the skin (also known as "sub-Q"-short for subcutaneous), or intravenously (through an IV). The common oral dosage ranges from 10 to 30 mg, with a maximum daily dose of about 40 mg. The subcutaneous dose is 0.25 mg every 20 to 60 minutes until a woman's contractions have subsided.
terbutaline dosage and route of administration
Since most of the uterus is made up of smooth muscle, the uterus will relax in response to a drug that contains substances like epinephrine.
terbutaline
heart disease, hyperthyroidism, and poorly controlled diabetes.
contraindications
It works by causing the uterus to contract. It is used to increase the strength of contractions of the uterus. It can be used during childbirth to speed delivery or after childbirth to control bleeding. It is also used clear the uterus after an incomplete abortion or miscarriage.Oxytocin (pronounced /ˌɒksɨˈtoʊsɪn/) is a mammalian hormone that also acts as a neurotransmitter in the brain.
pitocin
dinoprostone, prostaglandin E2
medicines for blood pressure
medicines used for sleep during surgery
other medicines to contract the uterus, ephedra
pitocin drug interactions
allergic reactions like skin rash, itching or hives, swelling of the face, lips, or tongue
breathing problems
excessive or continuing vaginal bleeding
fast, irregular heartbeat
feeling faint or lightheaded, falls
high blood pressure
seizures
unusual bleeding or bruising
unusual swelling, sudden weight gain
side effects that require immediate attention for pitocin
headache
nausea and vomiting
pitocin side effects
ntravenous infusion (drip method) is the only acceptable method of parenteral administration of Pitocin for the induction or stimulation of labor. Accurate control of the rate of infusion is essential and is best accomplished by an infusion pump. It is convenient to piggyback the Pitocin infusion on a physiologic electrolyte solution, permitting the Pitocin infusion to be stopped abruptly without interrupting the electrolyte infusion.
route of administration for pitocin
The initial dose should be 0.5-1 mU/min (equal to 3-6 mL of the dilute oxytocin solution per hour). At 30-60 minute intervals the dose should be gradually increased in increments of 1-2 mU/min until the desired contraction pattern has been established. Once the desired frequency of contractions has been reached and labor has progressed to 5-6 cm dilation, the dose may be reduced by similar increments.
pitocin dosage
Monitoring
a. Electronically monitor the uterine activity and the fetal heart rate throughout the infusion of Pitocin. Attention should be given to tonus, amplitude and frequency of contractions, and to the fetal heart rate in relation to uterine contractions. If uterine contractions become too powerful, the infusion can be abruptly stopped, and oxytocic stimulation of the uterine musculature will soon wane (see PRECAUTIONS section).

b. Discontinue the infusion of Pitocin immediately in the event of uterine hyperactivity and/or fetal distress. Administer oxygen to the mother, who preferably should be put in a lateral position. The condition of mother and fetus should immediately be evaluated by the responsible physician and appropriate steps taken.
Pitocin monitoring
Intravenous infusion (drip method). If the patient has an intravenous infusion running, 10 to 40 units of oxytocin may be added to the bottle, depending on the amount of electrolyte or dextrose solution remaining (maximum 40 units to 1000 mL). Adjust the infusion rate to sustain uterine contraction and control uterine atony.
Intramuscular administration, (One mL) Ten (10) units of Pitocin can be given after the delivery of the placenta.
control postpartum bleeding with pitocin
fetal distress, hydramnios, partial placenta previa, prematurity, borderline cephalopelvic disproportion, and any condition in which there is a predisposition for uterine rupture, such as previous major surgery on the cervix or uterus including cesarean section, overdistention of the uterus, grand multiparity, or past history of uterine sepsis or of traumatic delivery.
pitocin contraindications
Sterile Solution, an oxytocic,is indicated for aborting pregnancy between the 13th and 20th weeks of gestation as calculated from the first day of the last normal menstrual period and in the following conditions related to second trimester abortion.treatment of postpartum hemorrhage due to uterine atony which has not responded to conventional methods of management. Prior treatment should include the use of intravenously administered oxytocin, manipulative techniques such as uterine massage and, unless contraindicated, intramuscular ergot preparations. Studies have shown that in such cases, use resulted in satisfactory control of hemorrhage
Hemabate indications & drug class
An initial dose of 250 micrograms of HEMABATE Sterile Solution (1 mL of HEMABATE) is to be given deep, intramuscularly.The total dose of HEMABATE should not exceed 2 milligrams (8 doses).
Hemabate dosage and route
must be refrigerated at 2° to 8° C (36° to 46° F).Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
Hemabate administration
are generally transient and reversible when therapy ends. The most frequent adverse reactions observed are related to its contractile effect on smooth muscle.vomiting and diarrhea, approximately one-third had nausea, one-eighth had a temperature increase greater than 2° F, and one-fourteenth experienced flushing.
Hemabate side effects
HEMABATE may augment the activity of other oxytocic agents. Concomitant use with other oxytocic agents is not recommended.
hemabate drug interactions