Ref (type) | Population | Outcome, Interventions | Results and statistical analysis | Effect size | Favours |
Adverse effects | |||||
[105]
RCT |
5926 people with vascular disease who were intolerant to ACE inhibitors |
Withdrawal for any cause
1090/2954 (37%) with telmisartan 1143/2972 (39%) with placebo |
P = 0.22 |
Not significant | |
[105]
RCT |
5926 people with vascular disease who were intolerant to ACE inhibitors |
Hypotensive symptoms
29/2954 (1.0%) with telmisartan 16/2972 (0.5%) with placebo |
P = 0.05 |
Not significant | |
[105]
RCT |
5926 people with vascular disease who were intolerant to ACE inhibitors |
Doubling of serum creatinine
60/2954 (2.0%) with telmisartan 42/2972 (1.4%) with placebo |
Significance not assessed |
||
[105]
RCT |
5926 people with vascular disease who were intolerant to ACE inhibitors |
Hyperkalaemia (potassium >5.5 mmol/L)
111/2954 (4%) with telmisartan 49/2972 (2%) with placebo |
Significance not assessed |
||
[106]
RCT |
20,332 people with previous stroke and risk factors for vascular disease |
Withdrawal because of adverse effects
1450/10,146 (14%) with telmisartan 1127/10,186 (11%) with placebo |
P <0.001 |
Effect size not calculated | placebo |
[106]
RCT |
20,332 people with previous stroke and risk factors for vascular disease |
Withdrawal because of hypotension
393/10,146 (4%) with telmisartan 186/10,186 (2%) with placebo |
P <0.001 |
Effect size not calculated | placebo |