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Ilé / Ìforúkọsílẹ̀ ní Nàìjíríà / Suxamethonium Chloride Injection

Suxamethonium Chloride Injection

NAFDAC Reg. Rárá. 04-6811 · Oògùn

Forukọsilẹ pẹlu NAFDAC. Iforukọsilẹ ti nṣiṣe lọwọAs of 4 November 2026 · synced automatically from official sources.
Ọja
Suxamethonium Chloride Injection
Nọmba NAFDAC
04-6811
Ohun elo ti nṣiṣe lọwọ
Suxamethonium
Agbara
50 mg
Fọọmu
Solution for injection
Iwọn iṣakojọpọ
1 x 10's (in vials)
Olupese
Ko ṣe atokọ
Olubẹwẹ (oluranlowo)
Alpha Pharmacy and Stores (Nig) Ltd
Ti fọwọsi
28 Sep 2021
Ipò
Inactive Wo lórí NAFDAC ↗
Iforukọsilẹ wulo si
27 Sep 2026
Tani o ṣe itaniji
Kosi ikankan ti a rii.
Ijabọ Agbegbe
Kò sí
Àwọn àyẹ̀wò àsìkò
0

Nipa oogun naa: Suxamethonium: uses, dosage and brands worldwide

What we found

  • Suxamethonium Chloride Injection is on the NAFDAC register with an active registration (04-6811). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

How to use Suxamethonium Chloride Injection

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Serious warning: WARNING RIS K OF CARDIAC ARREST FROM HYPERKALEMIC RHABDOMYOLYSIS There have been rare reports of acute rhabdomyolysis with hyperkalemia followed by ventricular dysrhythmias, cardiac arrest and death after the administration of succinylcholine to apparently healthy pediatric patients who were subsequently found to have undiagnosed skeletal muscle myopathy, most frequently Duchenne’s muscular dystrophy. …
Tani o jẹ fun

Succinylcholine chloride is indicated as an adjunct to general anesthesia, to facilitate tracheal intubation, and to provide skeletal muscle relaxation during surgery or mechanical ventilation.

Bii o ṣe le mu u ati igba melo ni
  • The dosage of succinylcholine should be individualized and should always be determined by the clinician after careful assessment of the patient (see WARNINGS )
  • Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit
  • Solutions which are not clear and colorless should not be used
  • Risk of Medication Errors Accidental administration of neuromuscular blocking agents may be fatal
  • Store succinylcholine chloride injection with the cap and ferrule intact and in a manner that minimizes the possibility of selecting the wrong product
  • Adults: For Short Surgical Procedures The average dose required to produce neuromuscular blockade and to facilitate tracheal intubation is 0.6 mg/kg succinylcholine chloride injection given intravenously
  • The optimum dose will vary among individuals and may be from 0.3 to 1.1 mg/kg for adults
  • Following administration of doses in this range, neuromuscular blockade develops in about 1 minute; maximum blockade may persist for about 2 minutes, after which recovery takes place within 4 to 6 minutes
  • However, very large doses may result in more prolonged blockade
  • A 5 to 10 mg test dose may be used to determine the sensitivity of the patient and the individual recovery time (see PRECAUTIONS )
  • For Long Surgical Procedures The dose of succinylcholine administered by infusion depends upon the duration of the surgical procedure and the need for muscle relaxation
  • The average rate for an adult ranges between 2.5 and 4.3 mg per minute. …
Children
  • Safety and effectiveness of succinylcholine chloride have been established
  • In pediatric patient age groups, neonate to adolescent
  • There are rare reports of ventricular dysrhythmias and cardiac arrest secondary to acute rhabdomyolysis with hyperkalemia in apparently healthy
  • Pediatric patients who receive succinylcholine (see BOX WARNING )
  • Many of these
  • Pediatric patients were subsequently found to have a skeletal muscle myopathy such as Duchenne’s muscular dystrophy whose clinical signs were not obvious. …
Older adults

Clinical studies of succinylcholine chloride did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. …

Talk to a doctor first if
  • Succinylcholine is contraindicated in persons with personal or familial history of malignant hyperthermia, skeletal muscle myopathies and known hypersensitivity to the drug
  • It is also contraindicated in patients after the acute phase of injury following major burns, multiple trauma, extensive denervation of skeletal muscle, or upper motor neuron injury, because succinylcholine administered to such individuals may result in severe hyperkalemia which may result in cardiac arrest (see WARNINGS ). …
Medicines it may not mix with

Drugs which may enhance the neuromuscular blocking action of succinylcholine include: promazine, oxytocin, aprotinin, certain non-penicillin antibiotics, quinidine, β-adrenergic blockers, procainamide, lidocaine, trimethaphan, lithium carbonate, magnesium salts, quinine, chloroquine, diethylether, isoflurane, desflurane, metoclopramide and terbutaline. The neuromuscular blocking effect of succinylcholine may be enhanced by drugs that reduce plasma cholinesterase activity (e.g., chronically administered oral contraceptives, glucocorticoids, or certain monoamine oxidase inhibitors) or by drugs that irreversibly inhibit plasma cholinesterase (see PRECAUTIONS ). …

Warnings

Succinylcholine should be used only by those skilled in the management of artificial respiration and only when facilities are instantly available for tracheal intubation and for providing adequate ventilation of the patient, including the administration of oxygen under positive pressure and the elimination of carbon dioxide. The clinician must be prepared to assist or control respiration. To avoid distress to the patient, succinylcholine should not be administered before unconsciousness has been induced. In emergency situations, however, it may be necessary to administer succinylcholine before unconsciousness is induced. …

Àbájáde tí ó ṣeéṣe

Adverse reactions to succinylcholine consist primarily of an extension of its pharmacological actions. Succinylcholine causes profound muscle relaxation resulting in respiratory depression to the point of apnea; this effect may be prolonged. Hypersensitivity reactions, including anaphylaxis, may occur in rare instances. The following additional adverse reactions have been reported: cardiac arrest, malignant hyperthermia, arrhythmias, bradycardia, tachycardia, hypertension, hypotension, hyperkalemia, prolonged respiratory depression or apnea, increased intraocular pressure, muscle fasciculation, jaw rigidity, postoperative muscle pain, rhabdomyolysis with possible myoglobinuric acute renal fa …

Pregnancy and breastfeeding

Pregnancy: Risk Summary It is also not known whether succinylcholine can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Animal reproduction studies have not been conducted with succinylcholine chloride. Succinylcholine should be given to a pregnant woman only if clearly needed. The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. …

If you take too much

Overdosage with succinylcholine may result in neuromuscular block beyond the time needed for surgery and anesthesia. This may be manifested by skeletal muscle weakness, decreased respiratory reserve, low tidal volume, or apnea. The primary treatment is maintenance of a patent airway and respiratory support until recovery of normal respiration is assured. …

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2023-05-03.

Label for suxamethonium, the active ingredient registered with NAFDAC.

Check your pack of Suxamethonium Chloride Injection

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3 free checks left today Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Suxamethonium Chloride Injection

What is in Suxamethonium Chloride Injection?

Suxamethonium Chloride Injection contains Suxamethonium (50 mg), as solution for injection, according to its NAFDAC registration record.

Is Suxamethonium Chloride Injection registered with NAFDAC?

Yes. Suxamethonium Chloride Injection is listed on the NAFDAC register under registration number 04-6811, and its registration is active as of 4 November 2026.

Has Suxamethonium Chloride Injection been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Suxamethonium Chloride Injection in our automatically synced alert list.

How can I check that my pack of Suxamethonium Chloride Injection is genuine?

Run a free authenticity scan with the NAFDAC number 04-6811, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

How do I take Suxamethonium Chloride Injection?

Follow your prescription or the leaflet in your pack. The official label says: The dosage of succinylcholine should be individualized and should always be determined by the clinician after careful assessment of the patient (see WARNINGS ). Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit. Solutions which are not clear and colorless should not be us…

What is Suxamethonium Chloride Injection used for?

Succinylcholine chloride is indicated as an adjunct to general anesthesia, to facilitate tracheal intubation, and to provide skeletal muscle relaxation during surgery or mechanical ventilation. (Summarised from the official U.S. FDA label for suxamethonium. Always follow your doctor or pharmacist.)

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