Tricyclic antidepressants |
2.2 (2.0–2.3) |
(amitryptiline, doxepin, trimipramine, clomipramine) |
|
Anticholinergic effects, better alternatives exist |
|
First-generation (low potency) antipsychotics |
2.6 (2.4–2.8) |
(chlorpromazine, chlorprotixene, levoprometazine, prochlorperazine) |
|
Anticholinergic effects, extrapyramidal effects, risk of falls and cognitive impairment |
|
Long-acting benzodiazepines |
4.6 (4.3–4.9) |
(nitrazepam, flunitrazepam) |
|
Risk of accumulation, prolonged sedation, falls and fractures |
|
Strong analgesics |
1.1 (1.0–1.2) |
(propoxyphene, pethidine, opioids with spasmolytics) |
|
Poorly tolerated by elderly, propoxyphene has narrow therapeutic width |
|
Risk of sedation, confusion, falls and fractures |
|
First-generation antihistamines |
2.5 (2.3–2.6) |
(dexchlorphenamine, promethazine, alimemazine, hydroxycin) |
|
Anticholinergic effects, risk of “hangover” |
|
Long time oral use of theophylline |
0.5 (0.5–0.6) |
Risk of cardiac arrhythmias |
|
No documented effect on COPD or asthma in the elderly, better alternatives exist |
|
Carisoprodol (muscle relaxant) |
1.0 (0.9–1.1) |
Anticholinergic effects, poorly tolerated by elderly, risk of muscle weakness, falls and fractures |
|
Beta blocking agent + unselective calcium channel blocker |
0.6 (0.5–0.6) |
May lead to AV block and myocardial depression |
|
NSAID + warfarin (any concomitant use) |
0.3 (0.3–0.4) |
Risk of gastrointestinal bleeding due to impaired platelet function |
|
NSAID + ACE inhibitor or A2-blocker (any concomitant use) |
3.4 (3.2–3.6) |
Risk of drug induced renal failure |
|
NSAID + SSRI (any concomitant use) |
0.8 (0.7–0.9) |
Increased risk of gastrointestinal bleeding |
|
NSAID + diuretic (any concomitant use) |
2.4 (2.2–2.5) |
Reduced effect of diuretics |
|
Three or more psychotropic drugs (analgesics containing opioids, psycholeptics, hypnotics, antidepressants) for ≥3 months |
2.8 (2.6–3.0) |
Total |
24.7 (23.7–25.6) |