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Neonatal tremor, jitteriness, irritability, feeding problems and somnolence, which may represent a withdrawal-emergent syndrome, are reported. Saxagliptin Saxagliptin inhibits dipeptidylpeptidase-4 to improve insulin secretion and lower glucagon secretion. No information is on the market on using saxagliptin during breastfeeding or whether it passes into breast milk. Saxagliptin is finest prevented during both pregnancy and lactation till further information is out there. Rodent teratogenicity studies are typically reassuring as is restricted use (of all triptans) during pregnancy. It is suggested that if rizatriptan is used, breastfeeding is finest prevented for the subsequent 24 hours. Monoamine neurotransmitters are necessary for the event of the immature mind, and endogenous ranges are highly regulated by monoamine oxidase. Potentially, any change in enzyme exercise may have a profound impact on brain improvement. Some suggest discontinuing monoamine Maternal medication and the infant oxidase inhibitors even earlier than conception. Very small amounts of senna may be found in breast milk; these are too small to produce a scientific effect within the breastfed infant. Temporarily discontinuing maternal remedy should have little impact on the long-term therapeutic consequence of main hypercholesterolaemia and will avoid exposing the fetus/infant to medication at a critical time. There appears to be a big affiliation with omphalocoele and septal defects. Neonatal abstinence syndrome might occur in up to one-third of uncovered neonates which continues for at least a few months. Sertraline is present in breast milk in quantities which are affected by timing and size of the maternal dose. The breastfed toddler should be monitored for possible adverse results; giving the drug in the lowest efficient dose and avoiding feeds at times of peak drug ranges (7�10 hours after maternal dosing) could minimise exposure. No clinically significant cardiac results have been reported in numerous case reviews. Sitagliptin inhibits dipeptidylpeptidase-4 to improve insulin secretion and lower glucagon secretion. Rodent teratogenicity research are reassuring, and very restricted human use has to date generally been reassuring. No data is available on the use of sitagliptin during breastfeeding or whether it passes into breast milk. Sitagliptin is best avoided throughout both being pregnant and lactation until further info is on the market. Rodent research reveal increased risk of embryo- and fetotoxicity, gastroschisis and umbilical hernia. Sodium aurothiomalate is excreted into breast milk, however no convincing instances of toddler toxicity have been reported. Sodium aurothiomalate should be used during pregnancy and lactation only if the benefit justifies the potential perinatal danger. Virtually not considered one of the commonly used asthma medications are contraindicated during pregnancy, and given that breastfeeding protects in opposition to food allergic reactions, exclusive breastfeeding ought to be strongly inspired for so long as potential in such instances. Sotalol crosses the placenta (F/M ratio ~1), and it has been used to treat fetal tachyarrhythmia with a reasonably high response fee (flecainide and digoxin are maybe more effective). In one case, it was estimated that a breastfed infant acquired a 20�23% of the weight-adjusted maternal dose; though there were no opposed events in this toddler, it is recommended that any child uncovered to maternal sotalol is intently monitored. Considering the indications and dosing, one-off sufentanil use is unlikely to pose a clinically vital threat to the breastfeeding neonate. Large epidemiologic studies establish no proof of teratogenicity or an increased prevalence of antagonistic fetal outcomes. No information is available on the usage of sulindac during breastfeeding; other agents may be most popular, especially whereas nursing a new child or preterm infant. Maternal medication and the infant 601 Sumatriptan Only small amounts of sumatriptan cross the placenta, and it ought to pose only minimal threat to the fetus.

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Furthermore, the risks of a temporary cessation in statin therapy throughout being pregnant and lactation seem to be low. Published stories of use during pregnancy are restricted to case reports of intrathecal use, and plasma concentrations after administration by this route are less than 1% of these after oral administration. Neonatal seizures were famous in a single case the place the mother was taking eighty mg/kg/day orally (seizures are reported after withdrawal in adults). Use through the third trimester has been linked with marrow suppression within the neonate, but this can be reduced by modifying the maternal dose. In distinction, poorly managed inflammatory bowel illness is prone to lead to reduced fecundity, prematurity and low birthweight. Congestive cardiac failure is probably the only indication for this drug during pregnancy, and even then, there are alternate options with a better safety profile. Thiazide diuretics are excreted in low concentrations into breast milk but are usually thought of safe during breastfeeding. It is teratogenic in rodents, inflicting skeletal malformations, hydroureter and vascular abnormalities. Isolated medical reports of bleomycin (usually together with other anti-neoplastic drugs) in the course of the second and third trimesters are generally favourable. Neonatal leucopenia has been reported, but long-term follow-up of youngsters exposed in utero has not revealed abnormalities. Bleomycin ought to only be used throughout pregnancy and lactation if the benefit justifies the potential risk. Most uncovered infants present some signs of opioid withdrawal, with signs showing 12�48 hours after birth, peaking at 72�96 hours and lasting for 120�168 hours after buprenorphine although other elements influence on this. Animal and human knowledge counsel low teratogenicity although some do report increased cardiovascular abnormalities. In general, no results have been seen in exposed breastfed infants; nevertheless, one case report paperwork the onset of seizures in a 6-month-old breastfed toddler shortly after the start of maternal bupropion remedy (seizures are recognized to happen in adults taking the drug). Bupivacaine Bupivacaine is used widely for epidural or spinal anaesthesia throughout labour. Bupivacaine crosses the placenta in small amounts that increase when fetal acidosis occurs. Bupivacaine and its major metabolite are found in breast milk at clinically irrelevant levels after epidural administration. Its use is unlikely to pose a clinically significant threat to the breastfeeding neonate. The basic recommendation is that buspirone ought to be averted throughout pregnancy and lactation. Given the potential effects on the toddler at a vital stage, use is best prevented throughout being pregnant and lactation. Most authorities consider propylthiouracil preferable to carbimazole, particularly throughout lactation, due to the chance of neonatal hypothyroidism. Calcipotriol Only small amounts (5�6%) of this topical psoriatic treatment are absorbed systemically. Rodent teratogenicity has not been reported besides when administered at levels >7. Although the producer advises avoiding use during being pregnant, two evaluations contemplate it to be safe. Not solely are small quantities absorbed systemically, but switch of vitamin D into milk can be low and calcipotriol levels in breast milk would be anticipated to be negligible. Related drugs in this class cross the placenta and fetal renal effects (anuria and oligohydramnios) have been reported. It is used for treatment of postpartum haemorrhage secondary to uterine atony after failure to respond to ergometrine and oxytocin. Risks are biggest through the second and third trimesters by way of results on the fetal kidney, causing renal failure and oligohydramnios, but teratogenesis during the first trimester is also reported. Captopril is embryocidal and causes stillbirths in a variety of animals (sheep, rabbits, rats). Captopril is excreted into breast milk at very low concentrations and is compatible with breastfeeding. Like most cephalosporins, cefadroxil is 566 Maternal medication and the baby Gardiner et al. Cefradine quickly crosses the placenta and is discovered in the amniotic fluid within hours of maternal administration.

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Although the histopathologic features of this tumor resemble a dermatofibroma, it may be distinguished clinically by the young age of onset, large size and plaque-like morphology. The lesions are flesh-colored linear bands, that are usually horizontally oriented, slightly agency, and elevated above the skin surface. Infantile myofibromatosis: A evaluate of clinicopathology with views on new therapy choices. A new child with multiple fractures as first presentation of childish myofibromatosis. Orbital infantile myofibroma: a case report and clinicopathologic evaluation of 24 circumstances from the literature. Development of renal and iliac aneurysms in a baby with generalized childish myofibromatosis. Infantile myofibromatosis: two families supporting autosomal dominant inheritance. Congenital desmoid tumor of the scalp: a histologically benign lesion with aggressive scientific behavior. Multimodal treatment of youngsters with unresectable or recurrent desmoid tumors; An 11-year longitudinal observational examine. Pediatric aggressive fibromatosis: A retrospective evaluation of 13 sufferers and evaluation of the literature. Fibrous tumors in youngsters: imaging options of a heterogeneous group of problems. Sternocleidomastoid pseudotumor and congenital muscular torticollis in infants: a prospective study of 510 circumstances. Further documentation of spontaneous regression of childish digital fibromatosis. A clinicopathological research of 45 pediatric gentle tissue tumors with an admixture of adipose tissue and fibroblastic components, and a proposal for classification as lipofibromatosis. Expanding the phenotype of gingival hyperplasia � psychological retardation � hypertrichosis (Zimmerman-Laband) syndrome. Leiomyoma of the hand in a baby who has the human immunodeficiency virus: A case report. Juvenile xanthogranuloma, neurofibromatosis, and juvenile chronic myelogenous leukemia. Concomitant juvenile xanthogranuloma and cutaneous mastocytosis in a 3-year-old Swedish girl: case report and evaluate of the literature. Langerhans cell histiocytosis preceding the development of juvenile xanthogranuloma: a case and review of current developments. WiskottAldrich syndrome caused by a new mutation related to multifocal juvenile xanthogranulomas. Eruptive juvenile xanthogranuloma related to relapsing acute lymphoblastic leukemia. Juvenile xanthogranuloma: Forms of systemic disease and their clinical implications. The risk of intraocular juvenile xanthogranuloma: Survey of current practices and assessment of threat. Nonlipidized juvenile xanthogranuloma: A histologic and immunohistochemical research. Subcutaneous fats necrosis of the newborn complicating hypothermic cardiac surgery. Subcutaneous fat necrosis with in depth calcification after hypothermia in two newborn infants. Localized dystrophic periocular calcification: A complication of intralesional corticosteroid remedy for childish periocular hemangiomas. Fulminant metastatic calcinosis with cutaneous necrosis in a baby with end-stage renal disease and tertiary hyperparathyroidism. Familial tumoral calcinosis: from characterization of a uncommon phenotype to the pathogenesis of ectopic calcification.

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Cost-effectiveness of antenatal screening for neonatal alloimmune thrombocytopenia. Platelet reference ranges for neonates, defined utilizing knowledge from over 47,000 sufferers in a multihospital healthcare system. Pneumococcal infection A range of great bacterial infections are brought on by the encapsulated Gram-positive coccus, Streptococcus pneumoniae. It typically causes community-acquired pneumonia and is now the commonest cause of deadly or disabling bacterial meningitis. Penicillin remains the drug of choice besides in areas the place the minimal inhibitory focus for penicillin is now >2 micrograms/ml. Such sufferers must be supplied prophylactic antibiotics, as a end result of the present vaccines only provide safety from a few of the capsular forms of pneumococcal an infection. They may also profit from being given the multivalent plain polysaccharide vaccine when 2 years old, and such immunisation should also be offered to patients 2 weeks ahead of any deliberate splenectomy or chemotherapy. Products Plain polysaccharide vaccine: An unconjugated vaccine, energetic against 23 of the more commonly encountered capsular forms of pneumococcal infection, has been available for some years. Because this vaccine offers relatively little protection when given to kids underneath 2 years old, it has usually solely been supplied to adults and to older children thought of to be at particularly high risk of an infection. Conjugate vaccine: A new 13-valent conjugated protein�polysaccharide vaccine (active against the 1, three, four, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F and 23F strains) was introduced to be used in young kids in 2010. This has replaced the previous obtainable 7-valent conjugated vaccine which caused a 70% decrease in invasive pneumococcal disease in younger kids in 3 years. While instances due to vaccine-related serotypes fell by nearly 80%, disease was then largely brought on by the extra 6 serotypes which at the second are covered by 13-valent conjugated vaccine. Contraindications Avoid immunisation throughout an acute an infection and while pregnant. Anaphylaxis is extremely unlikely � its management is mentioned within the monograph on immunisation. Early trends for invasive pneumococcal infections in kids after the introduction of the 13-valent pneumococcal conjugate vaccine. Cost-effectiveness of pneumococcal conjugate vaccination within the prevention of kid mortality: a global financial evaluation. Effectiveness of seven-valent pneumococcal conjugate vaccine against invasive pneumococcal disease: a matched case-control study. Poliomyelitis Poliomyelitis is a notifiable infectious illness that has now been eradicated from many of the world, however circumstances were still being recorded in Afghanistan, Chad, Ethiopia, northern India, Indonesia, Pakistan, Nigeria and Yemen in 2005. The World Health Organization launched a worldwide 15-year plan to rid the world of this illness in 1988, and one nation � northern Nigeria � now accounts for nearly half of all the new instances being reported across the world each year. Infection may be clinically silent but can also produce aseptic meningitis and extreme lasting paralysis. An injectable formaldehyde-inactivated triple-strain (Salk) vaccine first grew to become obtainable in 1958; a stay, attenuated, triple-strain oral (Sabin) vaccine was introduced in 1962; and a more potent monovalent product was licensed to be used in India in 2005. The Salk vaccine is now the one product used in North America and getting used with rising frequency in most parts of Europe (the Sabin vaccine was nonetheless used within the United Kingdom until September 2004). The two products have, between them, certainly made the eventual global eradication of polio a practical purpose. Remember however that kids excrete the reside virus in their stools for up to 6 weeks after immunisation, placing other unimmunised and immunocompromised sufferers and family contacts at risk. There can be a one in one million likelihood of the reside, attenuated vaccine itself causing paralytic disease. Interactions Polio vaccine may be given at the same time as different live and inactivated vaccines. Poliomyelitis prevention: revised suggestions to be used of only inactivated poliovirus vaccine for routine immunisation. Protective efficacy of a monovalent oral kind 1 poliovirus vaccine: a case-control research. However, neither salbutamol nor glucose and insulin will remove potassium from the physique. Sodium and calcium polystyrene sulfonate are cation-exchange resins used to draw potassium out of the physique and into the intestine in change for sodium or calcium, thus effecting the elimination of potassium from the physique within the faeces. Calcium resin can be preferred if the plasma sodium degree is already excessive, because the sodium resin can exacerbate hypernatraemia, which if it becomes extreme (plasma sodium a hundred and sixty mmol/l) might trigger serious neurological harm. Each gram of sodium resin is succesful, in apply, of extracting about 1 mmol of potassium from the body (as a lot as 3 mmol in theory).

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Congenital brachydactyly and nail hypoplasia: clue to bone-dependent nail formation. Fetal development, main malformations, and minor anomalies in infants born to girls receiving valproic acid. Hypothetical mechanism for fetal alcohol syndrome involving ethanol inhibition of retinoic acid synthesis at the alcohol dehydrogenase step. Low serum focus of all-trans and 13-cis retinoic acids in sufferers handled with phenytoin, carbamazepine, and valproate: potential relation to teratogenicity. The nail�patella syndrome: clinical and genetic aspects of 5 kindreds with 38 affected relations. Hereditary onycho-osteodysplasia (the nail�patella syndrome) with nephrosis-like renal disease in a new child boy. Nail� patella syndrome in a spontaneously aborted 18-week fetus: ultrastructural and immunofluorescent examine of the kidneys. Nail� patella syndrome: a distinctive clinical and electron microscopic presentation. Prevalence and new phenotypic and radiologic findings in congenital onychodysplasia of the index finger. Congenital malalignment of the large toenail as a cause of ingrowing toenail in infancy: pathology and treatment (a research of thirty cases). A evaluate of the clinical phenotype of 254 patients with genetically confirmed pachyonychia congenita. Congenital malalignment of the fourth toenail with congenital curved nail of the contralateral fourth toe. Immunology of the human nail equipment: the nail matrix is a site of relative immune privilege. Subungual infection within the newborn: an institutional outbreak of unknown etiology, possibly due to Veillonella. Epidemiology of dermatophytoses in kids living in northeast France: a 5-year examine. Dermatophyte onychomycosis in children beneath 2 years of age: experience of 16 circumstances. Congenital candidal onychomycosis: effective treatment with ciclopirox olamine 8% nail lacquer. Superficial white onychomycosis of the fingernails in a 1-yearold baby with hypoxemia. Longitudinal melanonychia in youngsters: A medical and histopathologic examine of 40 instances. Progressive fading of a longitudinal melanonychia because of a nail matrix melanocytic nevus in a toddler. Childhood subungual melanoma in situ in diffuse nail melanosis beginning as increasing longitudinal melanonychia. Where previous dilution or a particularly slow price of infusion is essential, this is specified in the relevant drug monograph, and the reason given. Here terminal co-infusion (the mixing of two completely different infusates utilizing a faucet or Y connector sited as near the affected person as possible) is sometimes identified to be safe. In the most frequently encountered situations where such co-infusion is secure, a remark to that impact occurs in the relevant drug monograph. In all other conditions two totally different infusion sites must be used until recommendation to the contrary has been obtained from the local hospital pharmacy. Symbols and abbreviations: Cross references between monographs are marked by the Latin phrase quod vide (contracted to q. Others are taken up and concentrated in some or all body tissues, the whole quantity in Neonatal Formulary 7: Drug Use in Pregnancy and the First Year of Life, Seventh Edition. Drug storage and administration Safe drug administration is every bit as essential as secure and efficient drug prescribing. Such issues come up with specific frequency when physique weight enters into the calculation. Guidance on this is given within the individual drug monographs, with advice on prior dilution where necessary. Equal thought also needs to be given to the timing and frequency of drug administration.

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Effectiveness of antibiotics in preventing meningococcal illness after a case: systematic evaluation. Cystinosis Cystinosis, first described by Aberhalden in 1903, is a rare autosomal recessive metabolic disorder. Three scientific forms of this disorder are described based mostly on the age at diagnosis and diploma of cellular cystine deposition: infantile onset, adolescent onset and adult onset. Patients with childish cystinosis (the commonest and most severe) turn into symptomatic at 3�18 months of age with polyuria, followed by poor growth, photophobia and, if not diagnosed and treated, renal failure by age 6 years. The renal tubular dysfunction results in classic renal Fanconi syndrome with impaired reabsorption of glucose, phosphate, amino and natural acids and minerals. Renal phosphate losses result in vitamin D-resistant rickets; continual losses of sodium bicarbonate and potassium result in persistent acidosis and hypokalaemia. There are a selection of ophthalmic abnormalities of which the pathognomonic birefringent refractile corneal deposits are the first to appear. Pharmacology Mercaptamine is an amino thiol that depletes lysosomal cystine in a disulphide trade response with cysteine. Mercaptamine postpones, and in some cases, even prevents the deterioration of renal operate and the development of extra-renal problems. Treatment ought to be started as soon as the analysis of cystinosis is made and continued lifelong, even after renal transplantation, to defend the extra-renal organs. Excessively high doses can cause pores and skin lesions due to angioendotheliomatosis (these disappear if the dose is reduced). The oral drug has no impact on the corneal cystine crystal accumulation, most likely as a end result of inadequate intraocular levels; thus, an ophthalmic preparation can additionally be required. The best outcomes are obtained by (1) making an early analysis, (2) administering mercaptamine each 6 hours and (3) performing frequent assays of leucocyte cystine. Treatment Note: Treatment with these products ought to solely be initiated after consultation with a specialist nephrology advisory centre. Oral treatment: Begin with one-sixth to one-quarter of the anticipated maintenance dose, elevated progressively over 4�6 weeks. Best outcomes are obtained from 6 hourly dosing, but a practical strategy is to medicate as quickly as the child wakes and before the mother and father go to bed, with the other two doses given at intermediate instances to unfold out the medicine as close to every 6 hours as attainable. Eye drops: Mercaptamine eye drops are instilled into every eye 4 to six times a day (at least 2�4 hours apart). Monitoring therapy Leucocyte cystine ranges are used to determine dosing and compliance once the upkeep dose is achieved and every 3 months thereafter. Blood is obtained 5�6 hours after mercaptamine therapy with the aim to achieve levels <1 nmol/half-cystine/mg protein. The contents of the capsules may be sprinkled on food (milk, potatoes or starch-based foods) or added to formula milk. Prenatal analysis of cystinosis by quantitative measurement of cystine in chorionic villi and cultured cells. A multicentre randomised double masked clinical trial of a new formulation of topical cysteamine for the remedy of corneal cystine crystals in cystinosis. Pharmacology Meropenem is a carbapenem -lactam antibiotic energetic against a really wide range of Gram-positive and Gram-negative cardio and anaerobic bacteria that first got here into basic medical use in 1985. Methicillin-resistant staphylococci and Enterococcus faecium are immune to meropenem, as are some strains of Pseudomonas aeruginosa. Meropenem is excreted within the urine, principally unchanged, however partly as an inert metabolite. The elimination half-life in adults is only one hour, but slightly longer in kids 2�6 months old. The preliminary half-life within the time period baby is 2 hours and within the preterm child 3 hours, but the half-life falls considerably, no matter gestation, within 10�14 days of delivery. Meropenem has many of the similar properties, and most of the identical antagonistic results, as imipenem (q. It has not been in use so lengthy as imipenem and has not been as extensively studied, however the proof to date suggests that meropenem is less more doubtless to induce seizures than imipenem with cilastatin (c.

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Mydriatic eye drops dilate the pupil, whereas cycloplegics paralyse the ciliary muscle, allowing diagnostic or therapeutic procedures. High doses of mydriatics may cause adverse systemic side effects (including ileus). Many eye drops also include antimicrobial preservatives; one of the most common is benzalkonium chloride; nonetheless, these are greatest prevented due to their propensity to cause issues with the tear film, cornea and conjunctiva with long-term use (see commentary). Infections Conjunctival irritation through the first month of life (ophthalmia neonatorum or neonatal conjunctivitis) occurs in up to 1 / 4 of neonates. The most serious infections are those caused by Neisseria gonococcus and Chlamydia trachomatis. Chloramphenicol eye drops are still broadly used to deal with low-grade conjunctivitis (especially the place this seems to be because of staphylococcal or coliform infection). Gonococcal an infection might be finest handled with a single massive intravenous or intramuscular dose of ceftriaxone or ceftazidime (q. The mom should all the time be seen and treated as nicely when venereally acquired neonatal gonococcal or chlamydial infection is encountered. Pseudomonas infection, which is doubtlessly very dangerous, ought to be handled with gentamicin eye drops and acceptable systemic antibiotics under the supervision of a marketing consultant ophthalmologist. Look for keratitis or a corneal ulcer using fluorescein if in any doubt after first anaesthetising the cornea. Herpes conjunctivitis as a primary manifestation of generalised neonatal herpes an infection requires equally skilled management with topical and systemic aciclovir (q. A continual watery discharge is normally due to congenital nasolacrimal duct obstruction (a quite common condition that nearly all the time cures itself and infrequently needs therapy unless overt an infection supervenes). Steroids Steroid eye drops should solely be used under the supervision of a advisor ophthalmologist and after the exclusion of herpetic eye disease. They may be used to reduce irritation after eye surgery, including laser therapy of retinopathy of prematurity. Fundal examination and screening for retinopathy of prematurity Various antimuscarinic and sympathomimetic drops can be found to result in mydriasis (dilatation of the pupil) or cycloplegia (paralysis of the ciliary muscle of the eye) making examination easier. Antimuscarinics dilate the pupil and paralyse the ciliary muscle; they range in potency and period of action. The action of tropicamide lasts about 4�6 hours, that of cyclopentolate up to 24 hours, and that of atropine as much as 7 days. Topical anaesthetics Oxybuprocaine and proxymetacaine are broadly used topical local anaesthetics. Gentle strain on the duct within the inner nook of the eye could cease the drops draining into the nostril and into the blood. It could additionally be used in easy bacterial conjunctivitis however can also be used to treat trachomatous conjunctivitis in conjunction with oral azithromycin (q. Steroid eye drops: Various preparations can be found, and a few mixed with antibiotics. Cyclopentolate hydrochloride (in a solution containing benzalkonium chloride) is out there in zero. However, they value 25p every and their use is tough to justify in babies with a gentle (probably chemical) conjunctivitis. References (See additionally the relevant Cochrane reviews) Baudouin C, Labb� A, Liang H, et al. A meta-analysis of the efficacy of ocular prophylactic agents used for the prevention of gonococcal and chlamydial ophthalmia neonatorum. A managed trial of povidone-iodine as prophylaxis towards ophthalmia neonatorum. Chloramphenicol therapy for acute infective conjunctivitis in kids in main care: a randomised double-blind placebo-controlled trial. Relation of aplastic anemia to use of chloramphenicol eye drops in two international case-control research. A steady infusion will cause tolerance to develop and exposes babies to signs of opiate withdrawal. Fentanyl citrate is an artificial fat-soluble opioid developed as an analogue of pethidine and haloperidol in 1964. It is used to present fast short-lived ache relief throughout surgical procedure and through epidural anaesthesia in childbirth.