B-Dol Tablets

B-DOL contains caffeine, codeine phosphate, doxylamine succinate and paracetamol. Paracetamol acts as an analgesic (painkiller) and an antipyretic (lowers body temperature), codeine phosphate is an analgesic, doxylamine succinate is an antihistamine and caffeine is a mild stimulant. B-DOL is indicated for short-term treatment of pain associated with tension.

Do not take B-DOL

• if you are allergic to paracetamol, doxylamine succinate, codeine phosphate or caffeine, or any of the other ingredients of B-DOL (listed in section 6).
• if you are taking a medicine of the class known as Monoamine Oxidase Inhibitors (MAOIs, e.g. selegiline, moclobemide), which are used as antidepressants, or if you had taken any medicine of this group in the past 14 days.
• if you are taking other medicines containing codeine or any other paracetamol-containing medicines.
• if you have kidney or liver problems.
• if you have been told by your doctor that you have a metabolic disorder called acute intermittent porphyria. Signs include severe abdominal pain, constipation or diarrhoea, nausea and vomiting, and pain in your chest, legs or back.
• if you have recently had an operation on your bile duct (biliary tract).
• if you are an alcoholic.
• if you have had a head injury or been told by your doctor that you have increased pressure in your head. Signs of this include headaches, being sick (vomiting) and blurred eyesight.
• if you are having an asthma attack or have severe breathing problems.
• if you are pregnant or breastfeeding your baby.
• if you have been told by your doctor that your body metabolises codeine to morphine very quickly.

Do not share medicines prescribed for you with any other person. Always take B-DOL exactly as described in this leaflet or as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure. The usual dose is: Adults and children 12 years and older.

If you take more B-DOL than you should

In the event of overdosage, consult your doctor or pharmacist. If neither is available, contact the nearest hospital or poison centre.

If you forget to take B-DOL

If you forget to take a dose, take it as soon as you remember. Do not take a double dose to make up for a forgotten dose.

B-DOL can have side effects. Not all side effects reported for B-DOL are included in this leaflet. Should your general health worsen or if you experience any untoward effects while taking B-DOL, please consult your healthcare provider for advice.

If any of the following happens, stop taking/giving B-DOL and tell your doctor immediately or go to the casualty department at your nearest hospital:

• swelling of the hands, feet, ankles, face, lips and mouth or throat, which may cause difficulty in swallowing or breathing;
• rash or itching;
• fainting.

These are all very serious side effects. If you have them, you may have had a serious reaction to B-DOL. You may need urgent medical attention or hospitalisation.

Tell your doctor immediately or go to the casualty department at your nearest hospital if you notice any of the following:

• low number of white blood cells. Signs include: fever, chills, sore throat;
• low number of cells involved with blood clotting. Signs include: more or worse bruises than normal, small purple or red dots under your skin, nosebleeds or bleeding gums, black or bloody-looking bowel movements, red or pink urine;
• an excessive breakdown of red blood cells causing a type of anaemia. Signs include: tiredness, headaches, shortness of breath, dizziness, looking pale and yellowing of the skin and the whites of the eyes;
• low number of red blood cells, white blood cells and cells involved with blood clotting. Signs include: weakness, tiredness, skin problems such as rashes or bruising, rapid heart rate, shortness of breath;
• changes in mood, anxiety, feeling depressed, confusion;
• perceptions of having seen, heard, touched, tasted or smelled something that wasn't actually there;
• seizures;
• slowing down of the central nervous system. Signs include: slower heart rate and breathing, extreme confusion and memory loss and poor judgement;
• increased pressure in the head. Signs include headache, blurred vision, feeling less alert than usual and vomiting;
• blurred vision, constriction of the pupil of the eye;
• ringing in the ears;
• changes in the way your heart beats, drop in blood pressure when standing up making (causing light-headedness or fainting);
• yellowing of the skin, whites of the eyes and mucous membranes (jaundice);
• difficulty in urinating, inability to empty all the urine from your bladder;
• sudden drop in body temperature;
• skin rash or itching, which may include redness, hives (red itchy bumps), blisters, pustules or peeling of the skin (Toxic Epidermal Necrolysis) and bleeding in the lips, eyes, mouth, nose and genitals (Toxic Epidermal Necrolysis or Stevens-Johnson Syndrome);
• a red, scaly, widespread rash with bumps under the skin and blisters mainly localized on the skin folds, trunk, and upper extremities accompanied by fever at the initiation of treatment (Acute Generalised Exanthematous Pustulosis);
• a severe skin reaction known as DRESS syndrome can occur. Symptoms of DRESS include: skin rash, fever, swelling of lymph nodes and an increase of eosinophils (a type of white blood cells);
• Fixed Drug Eruptions (FDE) (may look like round or oval patches of redness and swelling of the skin), blistering (hives), itching.

These are all serious side effects. You may need urgent medical attention.

Tell your doctor if you notice any of the following:

Frequent side effects:

• Drowsiness;
• nausea, vomiting, constipation.

Less frequent side effects:

• severe stomach pain, which may reach to your back. This could be a sign of inflammation of the pancreas (pancreatitis).

Side effects with unknown frequency:

• dry mouth, sores in the mouth;
• changes in the way you move, talk or do regular activities;
• sleep disturbances;
• restlessness;
• decreased libido;
• lack of energy;
• dizziness;
• incoordination;
• headache;
• sensitivity to light;
• tingling or prickling, “pins-and-needles” sensation in the arms, hands, legs or feet;
• involuntary shaking of the hands, legs, face, head or vocal cords;
• thick phlegm;
• heartburn, diarrhoea, stomach pain, painful muscles;
• fever, sweating;
• hair loss;
• reddening of the face.

If you notice any side effects not mentioned in this leaflet, please inform your doctor or pharmacist.

Reporting of side effects

If you get side effects, talk to your doctor or pharmacist. You can also report side effects to SAHPRA via the “6.04 Adverse Drug Reaction Reporting Form”, found online under SAHPRA’s publications: https://www.sahpra.org.za/Publications/Index/8 . By reporting side effects, you can help provide more information on the safety of B-DOL.

• Store all medicines out of reach of children.
• Store at or below 25 °C, in a dry place.
• Protect from light. Keep containers well closed.
• Do not store in a bathroom.
• Do not use after the expiry date stated on the label or bottle.
• Return all unused medicine to your pharmacist.
• Do not dispose of unused medicine in drains or sewerage systems (e.g. toilets).