Download CMI (PDF)

Total Page:16

File Type:pdf, Size:1020Kb

Download CMI (PDF) PETHIDINE JUNO INJECTION Pethidine hydrochloride Consumer Medicine Information WARNINGS Limitations of use Because of the risks associated with the use of opioids, pethidine should only be used when your doctor decides that other treatment options are not able to effectively manage your pain or you cannot tolerate them. Hazardous and harmful use Pethidine poses risks of abuse, misuse and addiction which can lead to overdose and death. Your doctor will monitor you regularly during treatment. Life threatening respiratory depression Pethidine can cause life-threatening or fatal breathing problems (slow, shallow, unusual or no breathing), even when used as recommended. These problems can occur at any time during use, but the risk is higher when first starting pethidine, after a dose increase, if you are older, or have an existing problem with your lungs. Your doctor will monitor you and change the dose as appropriate. Use of benzodiazepines and other central nervous system (CNS) depressants, including alcohol Using pethidine with other medicines that can make you feel drowsy such as sleeping tablets (e.g. benzodiazepines), other pain relievers, antihistamines, antidepressants, antipsychotics, gabapentinoids (e.g. gabapentin and pregabalin), cannabis and alcohol may result in severe drowsiness, decreased awareness, breathing problems, coma and death. Your doctor will minimize the dose and duration of use; and monitor you for signs and symptoms of breathing difficulties and sedation. You must not drink alcohol while using pethidine. What is in this leaflet Before you are given PETHIDINE Tell your doctor or pharmacist if you are pregnant or intend to become pregnant. This leaflet answers some of the common When you must not be given it Your doctor or pharmacist will discuss the questions people ask about Pethidine Juno. It This medicine must not be given to you if possible risks and benefits of being given does not contain all the information that is you have an allergy to pethidine or any of pethidine during pregnancy. known about pethidine. the ingredients listed at the end of this Tell your doctor or pharmacist if you are It does not take the place of talking to your leaflet. breast-feeding or plan to breast-feed. doctor or pharmacist. Symptoms of an allergic reaction to Pethidine passes into breast milk and All medicines have risks and benefits. Your pethidine may include: therefore there is a possibility that your baby doctor has weighed the risks of you being • shortness of breath, wheezing or may be affected. Your doctor or pharmacist given pethidine against the benefits they difficulty breathing will discuss the possible risks and benefits of expect it will have for you. being given pethidine during breastfeeding. • swelling of the face, lips, tongue or other If you have any concerns about being parts of the body Tell your doctor or pharmacist if you have given this medicine, ask your doctor or any medical conditions, especially the • rash, itching or hives on the skin. pharmacist. following: Pethidine Juno should not be given to you Keep this leaflet. • lung or breathing problems if you: You may need to read it again. • a history of alcohol or drug abuse • have respiratory diseases such as severe • a history of mental illness What PETHIDINE is for emphysema, severe chronic bronchitis, kyphoscoliosis, acute asthma or chronic • under-active thyroid (hypothyroidism) Pethidine is a powerful drug used to relieve airway disease. and/or adrenal gland (Addison’s disease) pain and produce sleepiness. • are suffering from a head injury or brain • adrenal gland tumour It can be used for the short-term management tumour (phaeochromocytoma) of severe pain or it can be used before • are suffering from a convulsive state • a history of epilepsy, fits (seizures) or painful operations to reduce the pain that you such as status epilepticus or tetanus, or if head injuries. feel. It can also be used during childbirth to you have eclampsia or pre-eclampsia • glaucoma (increased pressure in the eye) ease the pain of contractions. • have an irregular heart beat (arrhythmia) • heart problems Pethidine belongs to a group of medicines called opioid (narcotic) analgesics. • have diabetic acidosis • severe liver or kidney impairment Pethidine works by changing the pain • are undergoing treatment with, or have • severe inflammatory bowel dsease or messages that are sent to the brain. finished treatment in the last two weeks biliary colic with, monoamine oxidase (MAO) • diabetes Your doctor will have explained why you are inhibitors eg selegeline, phenelzine, being treated with pethidine and told you tranylcypromine, moclobemide If you have not told your doctor or what dose you will be given. pharmacist about any of the above, tell • have severe liver disease Follow all directions given to you by your them before you are given Pethidine Juno. doctor carefully. • have blood-thinning problems, or are Taking other medicines They may differ from the information receiving treatment for this disorder (eg warfarin) You must tell your doctor if you are contained in this leaflet. taking any other medicines, including • are suffering from acute alcoholism. Your doctor may prescribe this medicine for medicines that you buy at the pharmacy, another use. Pethidine Juno should not be given to you supermarket or health food shop. after the expiry date (EXP) printed on the Ask your doctor if you want more Some medicines and pethidine may interfere pack. information. with each other. These include: If this medicine is used after the expiry date Pethidine can be addictive. The risk of has passed, it may not work as well. • antidepressants or medicines for anxiety addiction is increased in people with a disorders, such as: Pethidine Juno should not be given to you history of substance abuse or mental illness. - selective serotonin reuptake inhibitors if the packaging is torn or shows signs of The risk also increases the longer the drug is (SSRIs) or tampering. used and with higher doses. However, it is - serotonin and norepinephrine reuptake also important to keep your pain under If you are not sure whether you should inhibitors (SNRIs), control. Your doctor can advise you on how start therapy with pethidine, talk to your - tricyclic antidepressants (TCAs) to best manage this. doctor or pharmacist. - monoamine oxidase inhibitors This medicine is only available with a Before you are given it (MAOIs) ie moclobemide, phenelzine, doctor’s prescription. Tell your doctor or pharmacist if you have tranylcypromine any allergies to: • medicines used for migraines (triptans) • any other medicines • medicines used to prevent or treat • any other substances, such as foods, nausea and vomiting (5- HT3 receptor preservatives or dyes. antagonists) PETHIDINE JUNO INJECTION Published by MIMS March 2021 1 • selegeline, a monoamine oxidase While you are using it • dizziness, light headedness or inhibitor used to treat Parkinson’s unsteadiness disease Things you must not do • disorientation • alcohol Tell any other doctors, dentists, and • mood changes or hallucinations • warfarin, a medicine used to prevent pharmacists who are treating you that you are being given Pethidine Juno. • sweating blood clots • blurred vision • If you are about to be started on any new phenytoin or phenobarbital, medicines • dry mouth used to control fits or seizures medicine, tell your doctor, dentist or pharmacist that you are being given • nausea (feeling sick) and/or vomiting • other medicines which may make you Pethidine Juno. drowsy such as sleeping tablets, tablets • constipation. to calm your nerves, muscle relaxants, If you plan to have surgery that needs a These are the more common side effects of medicines to treat mental disorders, general anaesthetic, tell your doctor or pethidine. Mostly these are mild and short- other strong painkillers, some dentist that you are undergoing therapy lived. with Pethidine Juno. antihistamines, general anaesthetics If any of the following happen, tell your • amphetamines If you plan to become pregnant while you doctor or nurse immediately or go to are undergoing therapy with pethidine, Accident and Emergency at your nearest • cimetidine, a medicine used to treat tell your doctor or pharmacist. stomach ulcers and gastric reflux. hospital: Talk to your doctor or pharmacist about • slow or troubled breathing These medicines may be affected by these possibilities if you think they may • severe drowsiness or weakness pethidine, or may affect how well it works. bother you. You may need different amounts of your • slow or rapid heart rate Things you must not do medicine, or you may need to take/use • difficult in urinating different medicines. Your doctor or Do not give Pethidine Juno to anyone else, • itchy rash pharmacist will advise you. even if they have the same condition as • agitation Your doctor and pharmacist may have more you. Do not use Pethidine Juno to treat information on medicines to be careful with any other complaints unless your doctor • muscle twitching, jerking or fits or avoid while you are receiving Pethidine or pharmacist tells you to. (seizures) Juno. Do not stop using pethidine, or lower the • loss of consciousness. If you have not told your doctor about any dosage, without checking with your doctor These may be serious side effects. You may of these things, tell them before you are or pharmacist. need urgent medical attention or given any pethidine. If you have been using pethidine for more hospitalisation. than two weeks, you may experience Some people may get other side effects after How PETHIDINE is given unpleasant feelings if you stop it suddenly. being given pethidine. Your doctor will probably want you to How much is given gradually reduce the amount of pethidine you Tell your doctor if you notice anything else that is making you feel unwell. Your doctor will decide what dose of are using, before stopping it completely. pethidine you will receive. This depends on Do not drive or operate machinery while Do not be alarmed by this list of possible your condition and other factors, such as you are being given Pethidine Juno.
Recommended publications
  • Effects of Prophylactic Ketamine and Pethidine to Control Postanesthetic Shivering: a Comparative Study
    Biomedical Research and Therapy, 5(12):2898-2903 Original Research Effects of prophylactic ketamine and pethidine to control postanesthetic shivering: A comparative study Masoum Khoshfetrat1, Ali Rosom Jalali2, Gholamreza Komeili3, Aliakbar Keykha4;∗ ABSTRACT Background: Shivering is an undesirable complication following general anesthesia and spinal anesthesia, whose early control can reduce postoperative metabolic and respiratory complications. Therefore, this study aims to compare the effects of prophylactic injection of ketamine and pethi- dine on postoperative shivering.Methods: This double-blind clinical trial was performed on 105 patients with short-term orthopedic and ENT surgery. The patients were randomly divided into three groups; 20 minutes before the end of the surgery, 0.4 mg/kg of pethidine was injected to the first group, 0.5 mg/kg of ketamine was injected to the second group, and normal saline was injected to the third group. After the surgery, the tympanic membrane temperature was measured at 0, 10, 20, and 30 minutes. The shivering was also measured by a four-point grading from zero (no shiv- ering) to four (severe shivering). Data were analyzed by one-way ANOVA, Kruskal Wallis, Chi-square 1Doctor of Medicine (MD), Fellow of and Pearson correlation. Results: The mean age of patients was 35.811.45 years in the ketamine Critical Care Medicine (FCCM), group, 34.811.64 years in the normal saline group, and 33.1110.5 years in the pethidine group. Department of Anesthesiology and The one-way ANOVA showed no significant difference in the mean age between the three groups Critical Care, Khatam-Al-Anbiya (P=0.645).
    [Show full text]
  • The In¯Uence of Medication on Erectile Function
    International Journal of Impotence Research (1997) 9, 17±26 ß 1997 Stockton Press All rights reserved 0955-9930/97 $12.00 The in¯uence of medication on erectile function W Meinhardt1, RF Kropman2, P Vermeij3, AAB Lycklama aÁ Nijeholt4 and J Zwartendijk4 1Department of Urology, Netherlands Cancer Institute/Antoni van Leeuwenhoek Hospital, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands; 2Department of Urology, Leyenburg Hospital, Leyweg 275, 2545 CH The Hague, The Netherlands; 3Pharmacy; and 4Department of Urology, Leiden University Hospital, P.O. Box 9600, 2300 RC Leiden, The Netherlands Keywords: impotence; side-effect; antipsychotic; antihypertensive; physiology; erectile function Introduction stopped their antihypertensive treatment over a ®ve year period, because of side-effects on sexual function.5 In the drug registration procedures sexual Several physiological mechanisms are involved in function is not a major issue. This means that erectile function. A negative in¯uence of prescrip- knowledge of the problem is mainly dependent on tion-drugs on these mechanisms will not always case reports and the lists from side effect registries.6±8 come to the attention of the clinician, whereas a Another way of looking at the problem is drug causing priapism will rarely escape the atten- combining available data on mechanisms of action tion. of drugs with the knowledge of the physiological When erectile function is in¯uenced in a negative mechanisms involved in erectile function. The way compensation may occur. For example, age- advantage of this approach is that remedies may related penile sensory disorders may be compen- evolve from it. sated for by extra stimulation.1 Diminished in¯ux of In this paper we will discuss the subject in the blood will lead to a slower onset of the erection, but following order: may be accepted.
    [Show full text]
  • Post- Operative Pain- Relief
    PPoosstt-- OOppeerraattiivvee PPaaiinn-- RReelliieeff • Pain is often the patient’s presenting symptom. It can provide useful clinical information and it is your responsibility to use this information to help the patient and alleviate suffering. • Manage pain wherever you see patients (emergency, operating room and on the ward) and anticipate their needs for pain management after surgery and discharge. • Do not unnecessarily delay the treatment of pain; for example, do not transport a patient without analgesia simply so that the next practitioner can appreciate how much pain the person is experiencing. • Pain management is our job. Pain Management and Techniques • Effective analgesia is an essential part of postoperative management. • Important injectable drugs for pain are the opiate analgesics. Nonsteroidal anti-inflammatory drugs (NSAIDs), such as diclofenac (1 mg/kg) and ibuprofen can also be given orally and rectally, as can paracetamol (15 mg/kg). • There are three situations where an opiate might be given: pre- operatively, intra-operatively, post-operatively. •• Opiate premedication is rarely indicated, although an injured patient in pain may have been given an opiate before coming to the operating room. • Opiates given pre- or intraoperatively have important effects in the postoperative period since there may be delayed recovery and respiratory depression, even necessitating mechanical ventilation. (continued to next page) PPoosstt-- OOppeerraattiivvee PPaaiinn-- RReelliieeff ((ccoonnttiiinnuueedd)) • Short acting opiate fentanyl is used intra-operatively to avoid this prolonged effect. • Naloxone antagonizes (reverses) all opiates, but its effect quickly wears off. • Commonly available inexpensive opiates are pethidine and morphine. • Morphine has about ten times the potency and a longer duration of action than pethidine.
    [Show full text]
  • A Nurse with Pethidine Addiction
    Case Report Eur J Gen Med 2012;9(1):59-61 A Nurse with Pethidine Addiction Bilge Burçak Annagür ABSTRACT Pethidine is a synthetic opioid substance with high addiction potential. It is commonly used in medicine pre and postoperatively to relieve the pain. A Pethidine addiction generally starts as iatrogenic and may be a problem for the clinicians when there is a real pain. Its opioid analgesic usage is legal, yet it is possible that it can be abused by the health care workers and addiction may become a frequent case. In order to attract attention to this issue a case of a nurse who was given pethidine after an operation to ease her pain and whom addiction is developed was presented. When the medicines with high addiction potential are given for the treatment, the patients must be followed closely in terms of addiction and drug abuse. Key words: Addiction, nurses, pethidine Pethidin Bağımlılığı Gelişen Bir Hemşire ÖZET Pethidin bağımlılık potansiyeli yüksek sentetik opioid bir maddedir. Tıpta ameliyat öncesi hazırlık döneminde ve ameliyat sonrası ağrıların giderilmesinde sıklıkla kullanılmaktadır. Pethidin bağımlılığı genellikle iatrojenik olarak başlar ve gerçek bir ağrı nedeni olduğunda klinisyenleri zor durumda bırakabilir. Bir opioid analjezik olarak kullanımı yasal olan pethidinin sağlık çalışanları arasında kötüye kullanımı ya da bağımlılığı sık karşılaşılabilecek bir durumdur. Bu konuya dikkat çekmek amacıyla geçirdiği bir ameliyat sonrasında ağrılarını dindirmek için pethidin verilen ve pethidin bağımlılığı gelişen bir hemşire olgu sunulmuştur. Tedavi amacıyla verilen ve bağımlılık potansiyeli yüksek olan ilaçlar kullanıldığında kötüye kullanım ve bağımlılık açısından hastalar yakından izlenmelidir. Anahtar Kelimeler: bağımlılık, hemşireler, pethidin INTRODUCTION very few presentations about the psychiatric problems of Pethidine is a synthetic opioid substance with high addic- these drugs and the fact that they can develop addiction tion potential.
    [Show full text]
  • Treatment for Acute Pain: an Evidence Map Technical Brief Number 33
    Technical Brief Number 33 R Treatment for Acute Pain: An Evidence Map Technical Brief Number 33 Treatment for Acute Pain: An Evidence Map Prepared for: Agency for Healthcare Research and Quality U.S. Department of Health and Human Services 5600 Fishers Lane Rockville, MD 20857 www.ahrq.gov Contract No. 290-2015-0000-81 Prepared by: Minnesota Evidence-based Practice Center Minneapolis, MN Investigators: Michelle Brasure, Ph.D., M.S.P.H., M.L.I.S. Victoria A. Nelson, M.Sc. Shellina Scheiner, PharmD, B.C.G.P. Mary L. Forte, Ph.D., D.C. Mary Butler, Ph.D., M.B.A. Sanket Nagarkar, D.D.S., M.P.H. Jayati Saha, Ph.D. Timothy J. Wilt, M.D., M.P.H. AHRQ Publication No. 19(20)-EHC022-EF October 2019 Key Messages Purpose of review The purpose of this evidence map is to provide a high-level overview of the current guidelines and systematic reviews on pharmacologic and nonpharmacologic treatments for acute pain. We map the evidence for several acute pain conditions including postoperative pain, dental pain, neck pain, back pain, renal colic, acute migraine, and sickle cell crisis. Improved understanding of the interventions studied for each of these acute pain conditions will provide insight on which topics are ready for comprehensive comparative effectiveness review. Key messages • Few systematic reviews provide a comprehensive rigorous assessment of all potential interventions, including nondrug interventions, to treat pain attributable to each acute pain condition. Acute pain conditions that may need a comprehensive systematic review or overview of systematic reviews include postoperative postdischarge pain, acute back pain, acute neck pain, renal colic, and acute migraine.
    [Show full text]
  • 0 Cover Part Two\374
    PART TWO DEUXIÈME PARTIE SEGUNDA PARTE ﺍﳉﺰﺀ ﺍﻟﺜﺎﱐ 第二部分 ЧАСТЬ ВТΟΡАЯ - (...), [...] - (-)-3-hidroxi-N- (-)-(2R)-N-méthyl-1- fenacilmorfinán → Levophenacyl-morphan phénylpropan-2-amine → Levometamfetamine (-)-3-hidroxi-N- (-)-(3S,6R)-6- metilmorfinán → Levorphanol (dimethylamino)-4,4- (-)-3-hydroksymorfinan → Norlevorphanol diphenyl-3-heptanol → Betamethadol (-)-3-hydroksy-N- (-)-(3S,6R)-6- fenacylmorfinan → Levophenacyl-morphan (dimethylamino)-4,4- (-)-3-hydroksy-N- diphenyl-3-heptanol metylmorfinan → Levorphanol acetate (ester) → Betacetylmethadol (-)-3-hydroxymorphinan → Norlevorphanol (-)-(5R)-4,5-epoxy-3- (-)-3-hydroxy-N- methoxy-9α-methyl methylmorphinan → Levorphanol → Thebacon morphin-6-en-6-yl acetate (-)-3-hydroxynormorphinan → Norlevorphanol (-)-(5R,6S)-3-benzyloxy-4,5- (-)-3-hydroxy-N- epoxy-9a-methylmorphin- phenacylmorphinan → Levophenacyl-morphan 7-en-6-yl myristate → Myrophine (-)-3-hydroxytropane-2- (-)-(5R,6S)-4,5-epoxy carboxylat → Ecgonine morphin-7-en-3,6-diol → Normorphine (-)-3-idrossi-N- (-)-(5R,6S,14S)-4,5-epoxy- metilmorfinano → Levorphanol 14-hydroxy-3-methoxy- (-)-3-methoxy-N- 9a-methylmorphinan-6- methylmorphinan → Levomethorphan one → Oxycodone (-)-3-metil-2,2-difenil-4- (-)-(R)-4,5-epoxy-3- morfolinbutirilpirrolidina → Levomoramide methoxy-9a-methyl (-)-3-metoksy-N- morphinan-6-one → Hydrocodone metylmorfinan → Levomethorphan (-)-(R)-6-(dimethylamino)- (-)-3-metossi-N-metil- 4,4-diphenyl-3-heptanone → l-methadone morfinano → Levomethorphan (-)-(R)-N,α-dimethyl (-)-3-metoxi-N- phenethylamine → Levometamfetamine
    [Show full text]
  • 1. What Pethidine Tablets Are and What They Are Used for 2. Before You
    148x420 Layout 1/4/08 15:32 Page 1 148x420 Layout 1/4/08 15:32 Page 2 PACKAGE LEAFLET: INFORMATION FOR THE USER D05458 3. How to take Pethidine Tablets Reporting of side effects Always take this medicine exactly as your doctor If you get any side effects, talk to your doctor or Pethidine 50mg Tablets or pharmacist has told you. Check with your pharmacist or nurse. This includes any possible doctor or pharmacist if you are not sure. side effects not listed in this leaflet. You can also report side effects directly via Yellow Card Pethidine Hydrochloride This medicine is for oral use. Scheme. Website: www.mhra.gov.uk/yellowcard Adults: or search for MHRA Yellow Card in the Google Read all of this leaflet carefully before you Other medicines which may interact with 1-3 tablets (50-150mg) as a single dose. This may Play or Apple App Store. By reporting side effects take this medicine because it contains Pethidine Tablets are: be repeated if the doctor decides this is needed you can help provide more information on the important information for you • medicines for sleeping problems (sedatives) but it should not be repeated more often than safety of this medicine. and anxiety, such as chloral, diazepam, and • Keep this leaflet. You may need to read it every four hours. 5. How to store Pethidine Tablets again. barbiturates • CNS depressants (drugs that act on the Elderly and infirm patients: Keep this medicine out of the sight and reach of • If you have any further questions, ask your 1 tablet (50mg).
    [Show full text]
  • A Comparison of Tramadol and Pethidine Analgesia on the Duration of Labour: a Randomised Clinical Trial
    Australian and New Zealand Journal of Obstetrics and Gynaecology 2009; 49: 59–63 DOI: 10.1111/j.1479-828X.2009.00949.x OriginalBlackwell Publishing Asia Article A comparison of tramadol and pethidine analgesia on the duration of labour: A randomised clinical trial Maryam KHOOSHIDEH1 and Ali SHAHRIARI2 1Department of Obstetrics and Gynaecology, and 2Department of Anaesthesiology, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran Background: The ideal obstetric analgesia should provide analgesic efficacy without attenuation of uterine contractions. Aims: To compare the outcome of intramuscular administration of pethidine and tramadol in labour analgesia. Methods: One hundred and sixty full-term parturients were randomly assigned to two equal groups in active labour. Group P received 50 mg pethidine; and group T, 100 mg tramadol intramuscularly. Primary outcome measure was the duration of the labour. The analgesic efficacy, maternal side-effects, mode of delivery, maternal satisfaction and Apgar score as the secondary outcome were assessed. Results: The duration of labour was shorter in group T, for first stage (190 vs 140 min; P < 0.0001) and for second stage (33 vs 25 min; P = 0.001). There were no differences in Groups P and T with respect to median (7 vs 8) and maximum (7.5 vs 8) visual analog scores (VAS) for pain at 10 min and one hour after drug administration. Women in group P had lower VAS pain scores than those in group T in the second stage of labour (8 vs 9; P = 0/009). There was a significantly higher incidence of nausea and vomiting (35% vs 15%; P = 0.003) and drowsiness (80% vs 29%; P < 0.0001) in group P.
    [Show full text]
  • Pain Management
    Pain management Preeyaphan Arunakul MD FRCAT Department of Anesthesia Faculty of Medicine, Thammasat University Definition “An unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage.” Classification of pain by time • Acute pain - Pain less than 12 weeks • Chronic pain - Pain longer than 12 weeks Nociceptive Nonnociceptive Somatic Visceral Neuropathic Psychogenic sharp, dull Poorly localized, Burning, electrical -Rarely pure aching deep squeezing, (lancinating), -No nociceptive or crampy numbing, neuropathic mechanism allodynia, can be identified -Myofascial hyperalgesia -With sufficient -Metastatic -Small bowel psychogenic symptoms bone pain obstruction -Postsurgical -Carcinomatosis -Trigeminal neuralgia -Arthritis peritonii -Postherpetic neuralgia -Painful peripheral neuropathy NSAIDs -CRPS I,II Opioids TCA/SSRI -Phantom limb pain Muscle relaxants Gabapentin Aniline deriv. Opioids Anticonvulsants Antidepressants Multimodalities Interventions Antidepressants Psychological therapy Psychotherapy Interventions Multimodalities Acute Postoperative Pain ผู้ป่วยมีอาการปวดเฉียบพลัน “5th Vital sign” มีสาเหตุที่ท าให้เกิดอาการปวด รักษาสาเหตุ ประเมินระดับความปวด ไม่ต้องการ อาการปวดต้องการการรักษาหรือไม่ ประเมินซ ้าและบันทึก ต้องการ (PS ≥ 4 หรือปวดปานกลางขึ้นไป) เครื่องมือที่ใช้ประเมินความปวด รักษาโดยใช้ยา - VAS/VRS/NRS รักษาโดยไม่ใช้ยา - FACE/FLACCs รักษาแบบผสมผสาน - CHEOPS ไม่ได้ผล การรักษาได้ผลดีหรือไม่ ปรึกษาผู้เชี่ยวชาญ ได้ผลดี เกิด เกิดภาวะแทรกซ้อนจากการรักษาหรือไม่
    [Show full text]
  • Codeine and Its Alternates for Pain and Cough Relief* 2
    Bull. Org. mond. Sante Bull. Wid Hith Org. J 1969, 40. 1-53 Codeine and its Alternates for Pain and Cough Relief* 2. Alternates for Pain Relief NATHAN B. EDDY, M.D.,1 HANS FRIEBEL, Dr med.,2 KLAUS-J)RGEN HAHN, Dr med.3 & HANS HALBACH, Dr med. Dr-Ing. 4 This report-the second of a series on codeine and its alternates for pain and cough relief-contains a detailed evaluation of experimental and clinical data on newer sub- stances having analgesic properties comparable to and in approximately the same range as those ofcodeine. The data are discussed under the headings: analgesic effects in animals; clinical usefulness; side-effects with particular reference to dependence andabuse liability. CONTENTS CARISOPRODOL ............... 1 PRODILIDINE ........... ... .. 42 DEXTROPROPOXYPHENE ........... 6 INDANES .................. 44 DHYDROCODEINE ............... 22 PHTHALIMIDES ............... 44 ETHOHEPTAZINE ............... 24 PYRROLIDINES .......... .... 45 ETYMIDE.. .............. 29 SPECIFIC OPIATE ANTAGONISTS .... 45 FENYRAMIDOL ............... 32 Risum .................... 47 METOFOLINE. .............. 33 REFERENCES ............. ... 48 CARISOPRODOL 5 propanediol carbamate isopropyl carbamate) was evaluated initially for paralysis of the intact animal, After the discovery and development of mepro- depression of spinal reflexes, anticonvulsant effect bamate, further exploitation of the dicarbamate molecule resulted in the preparation of substances 0 which differed widely in their pattern of activity. CH3-CH2-CH2 CH2-O-C-NHCH (CH3)2 One of these, carisoprodol (2-methyl-2-propyl-1,3- \I/ c * This review of the analgesic and antitussive effects of CH3 CH2-0-C-NH2 codeine and its alternates is being published in the Bulletin of the World Health Organization in five instalments. The first, devoted to an assessment of codeine as a pain reliever, was published in Bull.
    [Show full text]
  • Comparison of Preoperative Tramadol and Pethidine on Postoperative
    Evangelista et al. BMC Veterinary Research 2014, 10:252 http://www.biomedcentral.com/1746-6148/10/252 RESEARCH ARTICLE Open Access Comparison of preoperative tramadol and pethidine on postoperative pain in cats undergoing ovariohysterectomy Marina C Evangelista*, Rodrigo A Silva, Larissa B Cardozo, Marcia A P Kahvegian, Thais C Rossetto, Julia M Matera and Denise T Fantoni Abstract Background: A variety of analgesic agents are available, and which one can be used in dogs and cats is a highly controversial issue, existing however a fear in the use of opiates due to possible adverse effects that these drugs can cause. The aim of this study was to compare the analgesic effect provided by the administration of tramadol or pethidine on early postoperative pain of cats undergoing ovariohysterectomy in a double-blind prospective study. Fourty-two animals were randomly assigned into three groups. Pet received pethidine (6 mg/kg), Tra 2 received tramadol (2 mg/kg) and Tra 4 received tramadol (4 mg/kg); all intramuscularly and associated with acepromazine (0.1 mg/kg). The efficacy of each analgesic regimen was evaluated prior to surgery (baseline - TBL), during surgery and 1, 3 and 6 hours after extubation with subjective pain scale, physiologic parameters, serum concentrations of glucose, cortisol and IL-6. Results: Changes in cardiovascular system were not clinically relevant. There were no significant differences in pain scores (P > 0.05) during the study, although the number of rescue analgesia was significantly higher (P < 0.05) at Pet group (5/14) than Tra 4 group (0/14), whereas in Tra 2, two animals (2/14) required additional analgesia.
    [Show full text]
  • Parenteral Pethidine for Labour Pain Relief and Substance Use Disorder: 20-Year Follow-Up Cohort Study in Offspring
    Open Access Research BMJ Open: first published as 10.1136/bmjopen-2011-000719 on 30 May 2012. Downloaded from Parenteral Pethidine for labour pain relief and substance use disorder: 20-year follow-up cohort study in offspring Robert Rodrigues Pereira,1,2,3 Humphrey Kanhai,4 Frits Rosendaal,5 Paula van Dommelen,6 Dick Swaab,7 Erik Rodrigues Pereira,8 Ben van de Wetering9 To cite: Rodrigues Pereira R, ABSTRACT ARTICLE SUMMARY Kanhai H, Rosendaal F, et al. Objective: To determine whether use of intrapartum Parenteral Pethidine for Pethidine pain analgesia increases the risk for Article focus labour pain relief and substance use disorder in adult offspring. - substance use disorder: Research question: does perinatal Pethidine for 20-year follow-up cohort Design: Analysis of data from a cohort study. labour pain relief lead to substance use disorder study in offspring. BMJ Open Setting: Academic hospital in Leiden, the Netherlands. in later life? 2012;2:e000719. doi:10. Participants: 133 cases and 164 control individuals, - Is it possible to confirm the published data on an 1136/bmjopen-2011-000719 aged 18e20 years at follow-up. OR of around 5? Main outcome measure: Incidence of substance use - We hypothesise that there is no relationship. < Prepublication history for disorder or use of alcohol and tobacco. this paper is available online. Key messages Results: The lifetime use of addictive substances in To view these files please - We cannot confirm earlier data on the risk of visit the journal online (http:// children exposed to intrapartum Pethidine analgesia substance use disorder after perinatal analgesia. dx.doi.org/10.1136/ was 45% of 133 children versus 48% of 164 not- - We did not find a risk for smoking and drinking bmjopen-2011-000719).
    [Show full text]