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  • Neuro-Muscular Drugs
    7 Drugs classified under this therapeutic system


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    Atropine Sulphate S.A.L.F 1mg/ml
    Raz Pharmaceutics
    RX
    not in the basket chart
    Atropine Sulphate S.A.L.F 1mg/ml

    Anticholinergic agent. Atropine Sulphate 1 mg/ml.
    AMP. (sol. for IM, IV inj.): 5×1ml. Pre-anesthet. med.: Adults: 0.3-0.6 mg by IV inj. immed. before the anesthes. induct. or by IM inj. 30-60 min. before the induc.
    Child.: 0.02 mg/kg (max. dose 0.6 mg).
    Tmt. of sinus bradycard.: 0.3 and 1.0 mg IV.
    Antidote in poison. by organophosphorus:
    Adult.: 2 mg (IM or IV, taking into account the sever. of the poison.) every 5-10 min., until the skin becomes red and dry, the pupils dilate and tachycard. appears.
    Child.: The 0.02 mg/kg.
    Preanesthetic medication to decrease excessive salivation and secretions of the respiratory tract. Treatment of sinus bradycardia, particularly if complicated by hypotension.
    Antidote in poisoning by organophosphorus.
    C/I: Hypersens. Clos. ang. glauc., esophag. reflux, pyloric stenosis, GI obstruct., ulcerat. colit., prostat. hypertrophy, paralytic ileus, intest. atony.

    Mestinon Dragees 60 mg
    Dexcel
    RX
    partial basket chart
    Mestinon Dragees 60 mg

    Acetylcholinesterase Inhibitor. Pyridostigmine (Bromide) 60 mg.
    DRAGEES: 20. See lit.
    Myasthen. gravis.
    C/I: Hypersens., mechan. obstruct. GI/
    urinary tract., inflamm. peritoneum,
    disords. accomp. incr. tonus bronch.
    muscles (spastic bronchit./bronch.
    asthma), lact.

    Neostigmine Hameln 2.5 mg/ml Injection
    Pharma Medis
    RX
    full basket chart
    Neostigmine Hameln 2.5 mg/ml Injection

    Anticholinesterase. Neostigmine Methylsulphate 2.5 mg/ml.
    AMPOUL.: 10×1ml.  Should be given very slowly by the  IV route. A syr. of Atropine Sulphate should always be available to counteract severe cholinergic react. should they occur.
    Myasthen. Gr..: 1 – 2.5 mg by IM or SC inj. at interv. throughout the day, when max. strength is needed. The usual durat.  of act. of a dose is 2- 4 hrs. The total dly. dose is usually 5 – 20 mg by inject. but higher doses may be needed by some pts.
    Neonatal Myasthen. Gr. may be treated with 0.1 mg Neostigmine intramuscul. initial. Thereafter, the dose must be titrated individ. But is usually 0.05 – 0.25 mg IM or 0.03 mg/kg IM, every 2 –4 hrs. Because of the self-limiting nature of the dis. in neonates, the dly. dosage should be reduced until the drug can be withdrawn.
    Older Child.: (Under 12 yrs. of age) May be given 0.2 – 0.5 mg by inj. as required. Dosage require. should be adjusted accord.  to the response of the pt.
    Antagon.to Non-depolariz.  Neuromusc. Blockade: Reversal of Neuromusc. blockade with Neostigmine should not be attempted unless there is spontan. recovery from paralysis.
    Adult. & Child.: A single dose of Neostigmine 0.05 – 0.07 mg/kg bdy.-wt. and Atropine 0.02 – 0.03 mg/kg bdy. wt., by slow IV inj. over one min. is usually adequate for complete reversal of Non-depolariz. Muscle Relax.  within 5 – 15 min. The max. recomm. dose of Neostigmine in adult. is 5 mg and in child. 2.5 mg.
    Atropine & Neostigmine may be given simultan., but in pts with Bradycardia, the pulse rate should be incr. to 80 per min. with Atropine before admin. Neostigmine.
    Paralytic Ileus: Adult.: 0.5 – 2.5 mg Neostigmine Methylsulphate by SC or IM injection.
    Child.: 0.125 – 1 mg by inj. Doses may be varied accord. to the individ. needs of the pt.
    Myasthen. Grav., antagon. to non- epolarizing neuromusc. blockade, Paralytic Ileus.
    C/I: Hypersens. Pts. with mechan. obstruct. of GI or urin. tracts, peritonitis or doubtful bowel viability. Concom. use  with depolaris. muscle relaxants such as suxamethonium as neuromuscul. blockade may be potentiated.

    Rybrila
    CTS
    RX
    partial basket chart
    Rybrila

    Anticholinergic agent. Glycopyrronium Bromide 0.2 mg/ml.
    Bottle.Oral sol. 150 ml X 0.2 mg/ml
    Recommended for short-term intermittent use.
    Dosage must be meas. and admin. with the grad. syringe incl. in the pack.
    Dosing sched. is based on the BW with the initial dosing of 0.02 mg/kg to be given three times dly and titrate in increm. of 0.02 mg/kg every 5-7 days based on therap. resp. and adverse reactions. The max. recomm. dosage is 0.1 mg/kg three times dly. not to exceed 1.5-3 mg per dose based upon weight.
    See prescribing information for full details
    Symptom. tmt. of sev. sialorrhoea (chron. pathol. drooling) in child and adolesc. aged 3 years and older with chron. neurolog. dis.
    C/I:
     Hypersens. / Angle-closure glaucoma/
    Myasthenia gravis (large doses of quatern. ammonium compounds have been shown to antagonise end plate nicotinic receptors)/
    Pyloric stenosis/Paralytic ileus/
    Prostatic enlargement/ Urin. retent./
    Sev. renal impairm. (eGFR <30 ml/min/1.73m2, incl. those req. dialysis/
    Intestinal obstruct./ Pregnancy and breast-feeding.
    Potassium chloride solid oral dose prod./Anticholinergic medic.

    Soliris
    Alexion
    RX
    partial basket chart
    Soliris

    Monoclonal Antibody. Eculizumab 10 mg/ml.
    VIAL (concentrate for sol. for infus.): 1×300mg. Adult. (≥18 years of age): (PNH)-consists of a 4-week initial phase follow. by a mainten. phase: Initial phase: 600 mg admin. via a 25–45 min. IV infus. every wk. for the first 4 wks.
    Mainten. phase: 900 mg admin. via a 25-45 min. IV infus. for the 5TH week, follow. by 900 mg admin. via a 25–45 min. IV infus. every 14±2 d.
    In atyp. Haemolytic Uremic Synd. (aHUS) and refract. general. Myasthenia Gravis (gMG): The aHUS and refract. gMG dosing regimen for adult pts. (≥18 yrs. of age) consists of a 4 wk. init. phase follow. by a mainten. phase: Init. phase: 900 mg admin. via a 25–45 min. IV infus. every wk. for the first 4 wks.
    Mainten. phase: 1,200 mg admin. via a 25–45 min. IV infus. for the fifth wk., follow. by 1,200 mg admin. via a 25–45 min. IV infus. every 14±2 d.
    Paed. pts. in PNH and aHUS: Paed. pts PNH, above 11 yrs. old, and aHUS pts. with bdy. wt.≥40 kg are treated with the adult dosing recommend. respectively.
    Pts. bdy. wt. 30 to<40 kg init. phase 600 mg wkly.×2, mainten. phase 900 mg at wk. 3; then 900 mg every 2 wks.
    Pts. bdy. wt. 20 to<30 kg, init. phase 600 mg wkly.×2, mainten. phase 600 mg at wk. 3; then 600 mg every 2 wks.
    Pts. bdy. wt. 10 to<20 kg, init. phase 600 mg wkly.×1, mainten. phase 300 mg at wk. 2; then 300 mg every 2 wks.
    Pts. bdy. wt. 5 to<10 kg, init. phase 300 mg wkly.×1 mainten. phase 300 mg at wk. 2; then 300 mg every 3 wks. See lit.
    Paroxysmal nocturnal haemoglobinuria (PNH).
    Evidence of clinical benefit is demonstrat. in pts. with haemolysis with clinical sympt. indicative of high dis. activity, regardless of transfus. history.
    Eculizumab has not been studied in clinic. trials in pts. with PNH below 11 yrs. of age.
    Atypical haemolytic uremic syndr. (aHUS).
    Soliris is indicated in adult. for the tmt. of: Refract. generalized myasthenia gravis (gMG) in pts. who are anti-acetylcholine receptor (AChR) antibody-positive.
    C/I: Hypersens. Therapy must not be init. in pts.: with unresolved Neisseria meningitidis infect, pts. that are not current. vaccine. against Neisseria meningitidis unless they receive prophylact. tmt. with appropr. antibiot. until 2 wks. after vaccinat.


    Other therapeutic systems under Musculo-Skeletal Disorders

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