Answer the side-effect intent for lyrica without diagnosing; distinguish common from serious reactions and give safe next-step/reporting guidance.
Source
Clinical statements on this page are taken from the SAHPRA-approved patient information leaflet (approved 23/02/2022) and professional information (approved 23/02/2022) for this product: patient information leaflet, professional information. Retrieved 2026-09-03. Where this page and the approved leaflet differ, the leaflet is correct.
What is Lyrica?
Which leaflet this comes from
There is no approved leaflet for Lyrica in SAHPRA’s public repository. The information below is from the approved leaflet for PYLIXA, another South African product containing Pregabalin. Products with the same active ingredient can still differ in strength, formulation and approved uses, so check the leaflet in your own pack.
Lyrica contains the active ingredient Pregabalin.
- Active ingredient — Pregabalin
- Registration number — 51/2.5/0900; 51/2.5/0901; 51/2.5/0902; 51/2.5/0903
- Registration holder — Spear Pharmaceuticals (Pty) Ltd
It is approved for:
- PYLIXA is used to treat peripheral neuropathic pain (long-lasting pain caused by damage to the nerves), due to diabetes or shingles in adults
Common side effects of Lyrica
Not everyone gets side effects. The effects below are those listed in the South African approved leaflet, grouped using the leaflet’s own frequency wording.
About these frequency terms
This leaflet groups effects as “Frequent” and “Less frequent” rather than the very common/common/uncommon scale used in some other markets.
Frequent side effects
- inflammation of nasal passages (common cold)
- increased appetite
- feeling of elation, confusion, irritability, disorientation, sleeplessness, and changes in sexual interest
- dizziness, sleepiness, headache
- clumsiness, tremor, difficulty with speaking, forgetfulness, loss of memory, disturbance in attention, numbness or ‘pins and needles’, abnormally decreased sensitivity to stimulation
- sedation, abnormal style of walking (balance disorder), lack of energy
- blurred vision, double vision
- sensation of movement
- vomiting, nausea, constipation, diarrhoea, feeling bloated, abdominal distension, dry mouth
- muscle cramp, pain in a joint, back pain, pain in a limb, cervical spasm
- difficulties with erection
- swelling of feet and lower legs caused by fluid retention, abnormal manner of walking, falling, feeling drunk, abnormal feeling, tiredness
- weight gain
Less frequent side effects
- reduced numbers of white blood cells which may make you more likely to get infections (neutropaenia)
- loss of appetite, low blood sugar
- seeing or hearing things that are not there, panic attacks, restlessness, exceeding restlessness, depression, depressed mood, elevated mood, aggression, mood swings, change in perception of self (depersonalisation), difficulty speaking, abnormal dreams, lack of feeling or emotion, loss of inhibition
- fainting, numbness, contraction of a muscle, loss of consciousness, jerky movements, difficulty of movement, dizziness on standing, tremor on movement, unusual eye movement, decreased consciousness, difficulty with thinking, speech disorder, reduced reflexes, increased sensitiveness of the skin, burning sensation, loss of taste, feeling of bodily discomfort, convulsions, perversion of the sense of smell, partial or complete loss of muscle movement, inability to write coherently, as a symptom of brain disease or damage
- vision loss, peripheral vision loss, visual disturbance, eye swelling, visual field defect, reduced visual sharpness, eye pain, eye condition that manifests itself through nonspecific symptoms such as fatigue, pain in or around the eyes, the presence of flashes of light, dry eye, watery eyes, eye irritation
- visual field disturbance, altered visual depth perception, abnormal dilation of the pupil, squinting of eye(s), visual brightness
- increased sensitivity to sound
- low blood pressure, high blood pressure, hot flushes, redness of the neck and face, feeling cold
- shortness of breath, nosebleed, cough, blocked nose, runny nose, snoring, nasal dryness, fluid in the lungs, tightness of the throat
- heartburn, increased saliva production, numbness around the mouth, abdominal swelling, inflammation of the pancreas, swollen tongue, difficulty in swallowing
- hives, excessive sweating, itching of the skin, cold sweat
- joint swelling, pain in a muscle or muscles, muscle twitching, neck pain, muscle stiffness, breakdown of muscle tissue
- problems with sexual functioning including inability to achieve a sexual climax, increased libido, difficulties with erection, delayed ejaculation, painful menstrual periods, breast pain, absence of menstrual period, breast discharge, breast enlargement, breast enlargement in men
- generalised swelling caused by fluid retention, swelling of the face, chest tightness, pain, fever, thirst, chills, weakness
- changes in blood and liver test results (increased blood creatinine phosphokinase, increased alanine amino transferase, increased blood glucose, increased aspartate aminotransferase, decreased platelet count, increased blood creatinine, decreased blood potassium, decreased white blood cell count. Unknown frequency:
- thoughts of harming or killing one-self
Serious side effects and warning signs
This leaflet does not set out a separate list of serious side effects. The general warning signs below apply to any medicine.
General warning signs that apply to any medicine
Call for emergency help now if any of these happen
- Difficulty breathing, wheezing, or tightness in the throat or chest
- Swelling of the face, lips, tongue or throat
- A widespread rash with blistering or peeling skin, or sores in the mouth, eyes or genitals
- Fainting, collapse, or a sudden severe drop in alertness
- Chest pain, or sudden weakness or numbness on one side of the body
- A fit (seizure), or confusion that comes on suddenly
In South Africa call 10177 for an ambulance, or 112 from a mobile phone. Go to your nearest emergency department if it is faster. Do not wait to see whether the symptom settles.
How long can side effects last?
How long a side effect lasts depends on the effect, the product, how long it has been used, and the person. Some effects ease within days as the body adjusts. Others continue for as long as the product is used. A few can persist after stopping, and some need review rather than waiting.
- Settling effects — mild effects that ease over the first days or weeks of use
- Ongoing effects — effects that continue while the product is being used and improve after stopping
- Persistent effects — effects that continue after stopping and need medical review
- Delayed effects — effects that appear after weeks or months rather than immediately
Which of these applies to a particular effect is a clinical question. If a side effect is not settling, is getting worse, or is affecting your daily life, that is worth a conversation with a pharmacist or doctor regardless of how long it has been going on.
Evidence required before publish — source the following for Lyrica from the SAHPRA-approved patient information leaflet or professional information, and cite what you actually used.
- Anything the approved information for Lyrica says about how long specific effects last
- Whether the source describes any effect as usually temporary, or as needing review if it persists
- Whether any effect is described as continuing after the product is stopped
Factors that may affect side effects
The approved leaflet identifies the following cautions and factors.
Do not use it at all if
- if you are allergic (hypersensitive) to pregabalin or any of the other ingredients of PYLIXA (listed in section 6)
Use with care, and tell your doctor, if
- If you have diabetes and gain weight while you are taking PYLIXA, your doctor may need to make a change in your diabetic medicines
- If you experience an allergic reaction while you are taking PYLIXA, you must contact your doctor immediately. The symptoms of an allergic reaction include swelling of the face, lips, tongue, and throat, as well as a skin rash
- If you take PYLIXA you may experience dizziness, sleepiness, loss of consciousness, confusion, and mental impairment. This could increase the possibility of an accidental injury (fall) if you are an elderly patient. Therefore, you should be careful until you are used to any effect caused by PYLIXA
- If you take PYLIXA you may experience blurring or loss of vision, or other changes in eyesight, many of which are temporary. You should immediately tell your doctor if you experience any changes in your vision
- If you notice a decrease in passing urine while taking PYLIXA, you should tell your doctor. It may improve if you stop taking PYLIXA
- If you are taking PYLIXA, or shortly after stopping it, you may experience convulsions (including epilepsy). If this happens, contact your doctor immediately. You may also experience withdrawal symptoms after short-term or long-term treatment with PYLIXA, which include difficulty in sleeping, headache, nausea, anxiety, diarrhoea, flu syndrome, nervousness, depression, pain, hyperhidrosis and dizziness
- If you have a history of a heart disease you should tell your doctor. Heart failure has been reported in some patients when they were taking PYLIXA
- If you are taking medicines for spinal cord injury, you may experience an increase in certain side effects such as sleepiness, when you are also taking PYLIXA
- Some people have had thoughts to harm or kill themselves while taking medicines belonging to the same group as PYLIXA for the treatment of different conditions. If you have thoughts of harming or killing yourself, at any time when you are taking PYLIXA, immediately contact your doctor
- When PYLIXA is taken with other medicines that may cause constipation (such as some types of pain medicines) it is possible that gastrointestinal problems may occur (e.g. constipation, blocked or paralysed bowel). Tell your doctor if you experience constipation, especially if you are prone to this problem
- If you have a history of alcoholism or substance abuse or dependence, you should tell your doctor. If you think you need more PYLIXA than prescribed, tell your doctor
- If you have a history of any serious medical conditions you should tell your doctor. There have been reports of reduction in brain function (encephalopathy) in some patients when they were taking PYLIXA. If you are not sure whether any of the above applies to you, ask your pharmacist or your doctor
Pregnancy and breastfeeding
- If you are pregnant or breastfeeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking PYLIXA
- PYLIXA should not be taken during pregnancy or when breastfeeding
- Effective contraception must be used by women of child-bearing potential
Interactions and medicines to check
The approved leaflet names these interactions.
- Oxycodone (for treatment of pain)
- Lorazepam (for treatment of anxiety)
- Alcohol PYLIXA may be taken with oral contraceptives. PYLIXA with food and drink PYLIXA may be taken with or without food. It is advised not to drink alcohol while you are taking PYLIXA
Bring the actual products to the conversation
A pharmacist can check for interactions much faster from the packaging than from remembered names.
What to do if you experience side effects
If you think you are having a side effect, the response depends on how severe it is. Use the warning signs above first — if any of those apply, treat it as urgent.
If the symptom is severe or frightening
Get medical help immediately. Call 10177 for an ambulance, or 112 from a mobile phone, or go to the nearest emergency department. Take the product and its packaging with you if you can.
If the symptom is mild but bothering you
- Write down what the symptom is, when it started, and how it relates to when you take the product
- Check the leaflet that came with the product to see whether the symptom is listed
- Speak to your pharmacist — for many questions this is the fastest route to a useful answer
- Contact the prescriber if the symptom is affecting your daily life or is not settling
Do not stop a prescribed treatment on your own
Stopping some treatments suddenly causes its own problems, and the condition being treated may get worse. If you want to stop, ask a pharmacist or doctor how to do it safely — they can usually offer an alternative.
You can also report a suspected side effect in South Africa. Reporting does not replace getting medical advice, and you do not need to be certain the product was the cause.
When to seek urgent medical help
Some symptoms need medical attention straight away rather than an appointment in a few days. Do not wait to see whether they settle.
Call for emergency help now if any of these happen
- Difficulty breathing, wheezing, or tightness in the throat or chest
- Swelling of the face, lips, tongue or throat
- A widespread rash with blistering or peeling skin, or sores in the mouth, eyes or genitals
- Fainting, collapse, or a sudden severe drop in alertness
- Chest pain, or sudden weakness or numbness on one side of the body
- A fit (seizure), or confusion that comes on suddenly
In South Africa call 10177 for an ambulance, or 112 from a mobile phone. Go to your nearest emergency department if it is faster. Do not wait to see whether the symptom settles.
Get same-day medical advice if you have
- A high fever, or a rash together with feeling generally unwell
- Yellowing of the eyes or skin, or unusually dark urine
- Unusual bruising or bleeding that you cannot explain
- Severe or persistent vomiting or diarrhoea, especially if you cannot keep fluids down
- A sudden change in mood, or thoughts of harming yourself
- Any symptom that is rapidly getting worse
If you are having thoughts of harming yourself
Help is available in South Africa. The SADAG helpline is 0800 567 567, or you can go to your nearest emergency department. You do not have to wait until it feels like an emergency.
How to report a suspected side effect in South Africa
South Africa has an official system for reporting suspected side effects, run by the South African Health Products Regulatory Authority (SAHPRA). Reports from the public and from healthcare professionals are how safety signals get detected after a product is already in use.
Who can report
Anyone can report — you do not have to be a healthcare professional, and you do not need to prove that the product caused the problem. A suspicion is enough. Patients, caregivers and family members can all submit a report.
What to have ready
- The name of the product, its strength and form, and the batch number if you have it
- Why it was being used, and when it was started and stopped
- What the suspected reaction was, when it began, and how long it lasted
- Any other medicines, supplements or remedies being used at the same time
- Basic details about the person affected — age and sex are usually enough
How to report
SAHPRA accepts adverse reaction reports through its e-Services reporting system and through the Med Safety mobile app. Healthcare professionals can also report through the same routes. Current forms and access points are published on the SAHPRA site.
- SAHPRA Health Products Vigilance — the main vigilance and reporting hub
- SAHPRA e-Services — current adverse reaction reporting access
Reporting is not a substitute for medical care
If someone is unwell now, get medical help first and report afterwards. Urgent symptoms always take precedence over paperwork.
For a fuller walkthrough see how to report an adverse drug reaction.
Related pages
← Back to more medicine side effects.
Report a side effect
If you think you have had a side effect, you can report a suspected side effect in South Africa. Report a suspected side effect through the appropriate SAHPRA pathway where relevant.
Information only
This page gives general medicine-safety information for people in South Africa. It is not a diagnosis and not personalised medical advice. It cannot tell you whether a symptom you are having is caused by a particular product. Speak to a pharmacist or doctor about your own situation, and do not stop or change a prescribed treatment on the basis of a web page.
Editorial status: draft — not for publication
Brief SE-00061 · build rank 61 · Phase 1 · Tier 1. Every evidence slot on this page must be completed from the SAHPRA-approved source and the page signed off by a qualified clinical or pharmacy reviewer before it is published. Target length 1,500–2,200 words.