6.1.15 Recognises adverse ocular reactions to medication. Flashcards
(32 cards)
Antidepressants (anti-psychotics produce more severe affects)
- Mydriasis
- Cycloplegia - blurred vision, reduced accommodation & convergence
- Dry eye
Antihistamines
- Dry eye & more staining
- Slight mydriasis - slight blurred vision
Anti-tuberculosis e.g. Ethambutol
Optic neuritis, Constriction of VF
Hydroxychloroquine
- Vortex keratopathy
- Bull eyes maculopathy (irreversible) - pigmentary changes/damage to macula
Tamoxifen
- Crystalline retinopathy
- Whorl-like corneal opacities
- Posterior subcapuslar opacities
- VF & CV changes
Prednisolone
- Steroid glaucoma (increased pressure)
- Steroid cataract - posterior subcapsular
- Corneal thinning
- Retard wound healing
Vigabatrin
- Bilateral constriction of VF
- Possible optic atrophy
- Reduced VA, CV defect
Alendronic acid
Eye inflammation - scleritis & keratitis
Tamsulosin
- Floppy iris syndrome
- Photophobia, visual disturbance
Sildenafil citrate (viagra)
Photophobia, Blurred vision, Conj hyperaemia, Ocular pain, CV defects
Amiodarone
- Corneal deposits - vortex keratopathy
- Len deposits - white-yellow punctates
- Optic neuropathy - rare!
Anti-malarials
e.g. Chloroquine, Mefloquine
Ocular side effects:
greyish-white corneal deposits (mainly subepithelial, whorl-like opacities)
blurred vision
pigmentary changes to retina
“Bull’s eye maculopathy”
VF loss
central/paracentral scotoma
Colour vision defects
Anti-inflammatories
NSAIDs e.g. Diclofenac, Ibuprofen, Indometacin
Ocular side-effects:
Dry eyes,
transient blurred vision, refractive changes
colour vision disturbance
Indometacin: pigmentary changes at the macula, corneal opacities, optic neuritis
Corticosteroids – Lots! (see lectures 1 & 14)
Hypnotics
Benzodiazepines e.g. Diazepam (Valium), Alprazolam (Xanax)
Ocular side-effects:
Reduced accommodation
EOM dysfunction
diplopia
allergic conjunctivitis
Oral contraceptives
E.g. Ethinyloestradiol/norethisterone
Ocular side effects:
Tear quality/quantity
Some reports of contact lens intolerance due to reduced tear secretion.
Retinal vein occlusion
What factors determine whether an ADR will occur?
- Age
- Sex
- Weight
- General/ophthalmic health
- Genetics (e.g. race)
- Dosage
- Duration of medication
- Concurrent medication
How would you recognise an ADR in practise?
- It would match with information you already know e.g. amiodarone causing vortex keratopathy.
- You MUST rule out other possible causes of the side effect before you can be sure!
- For example, if patient has started new medication & is reporting dry eyes, not reported before, then you can suspect the medication but you must also rule out other conditions/possibilities such as dry eye conditions, hormones, recent starting of CL wear, GH condition.
- Ask if it’s worsening and exactly when it started i.e. if started very soon after medication has been taken then a likely possibility. You would also need to conduct a full dry eye assessment
- You MUST rule out other possible causes of the side effect before you can be sure!
What patient groups do you need to take particular care with when considering topical medication?
At-risk groups such as very young or very old patients, those with renal (kidney) or hepatic (liver) impairment or patients who are pregnant or breastfeeding.
How do you check the risk of the drugs you are instilling?
- Consider if a drug will interact with another e.g. phenylephrine may interact with systemically administered monoamine-oxidase inhibitors and anti-hypertensive drugs.
- Check Van hericks & IOPs before & after dilation
- Ensure awareness to px that they may not be able to drive for few hours if mydriatic used
- Check corneal integrity if needed
- You should ask the patient if they:
have experienced adverse reactions to eye drops in the past
have a history of drug-induced adverse incidents
have any relevant medical conditions
take any systemic drugs. - You should check:
that you are administering the correct drug and dosage
the expiry date. - You should record all drugs used, including the batch number and expiry date, on the patient record.
What should you explain to the px before instilling any drugs?
- why you are instilling the drug
- what effects the drops might have
- how long the effects might last
- the side effects they might experience
- if you are dilating their pupils, that they might not be able to drive and must not undertake
- any activity which is not advised after dilation, and for how long
- if you are using anaesthetic drops, that they should avoid wearing contact lenses for an
- appropriate period of time after anaesthesia
- what to do if they experience an adverse reaction.
Give them a drug leaflet
What advice is given for if the px experience an ADR?
- You should tell the patient to attend the local Accident and Emergency department if you are not available to deal with any emergency or adverse reaction that may arise following the instillation of the drug
- Ensure to tell the patient what ADRs may occur
- You should inform the patient’s GP of any suspected adverse reaction
- In MOST situations, the ADR will be mild & can be seen routinely by GP & whatnot. In these cases, DO NOT tell the px to stop using the medication or lower the dosage. You have NO RIGHT to do so. If you do, you’re legally liable for any further consequences as a result. YOU MUST advise px not to stop using until seen by relevant medical professional i.e. doctor. MAKE SURE to record this in the notes!
Reporting Schemes
- You should use reporting schemes for adverse drug reactions . There are two reporting schemes, operated by the MHRA. These are:
1. the yellow card scheme which covers systemic adverse reactions to ocular medicines and ocular reactions to systemic medication
2. the Medical Devices Reporting Form which covers adverse incidents mainly relating to contact lenses and care products, including contact lens comfort drops
How to report?
- Online form - www.mhra.gov.uk/yellowcard
- On paper –
- complete a paper Yellow Card form post to: FREEPOST YELLOW CARD
- Yellow Cards forms are in the back pages of the BNF & MIMS
What to report?
The side effect(s).
Info about the px
The name of the drug
Your name and address