ARV Adverse Effects & Drug Classes
- Frequent effects (events expected in at least 10% of treated individuals) (bold-black)
- Severe effects (events that can put a person's life at risk and represent a medical emergency) (orange)
- Neither frequent nor severe effects (black)
NRTIs
Drug | Adverse Effect(s) |
---|---|
3TC | |
FTC | |
TDF(i) | Hepatitis ↓ BMD Osteomalacia ↑ Fractures risk ↓ eGFR Fanconi syndrome |
TAF(i) |
Weight gain |
ABC |
Rash Nausea* Diarrhoea* Coronary heart disease *Systemic hypersensitivity syndrome (HLA B*57:01 dependent) |
ZDV(ii) |
Nail pigmentation |
* Refers to effects seen in relation to hypersensitivity reactions
NNRTIs
Drug | Adverse Effect(s) |
---|---|
EFV |
Rash |
RPV |
Rash |
DOR | Sleep disturbance Headache |
ETV |
Rash |
NVP | Rash* Hepatitis* *Systemic hypersensitivity (CD4 count and gender dependent) |
* Refers to effects seen in relation to hypersensitivity reactions
PIs
Drug | Adverse Effect(s) |
---|---|
DRV(iv) |
Rash |
ATV(iv) |
Nausea and Diarrhoea(v) |
LPV | Nausea and Diarrhoea(v) IHD ↓ eGFR Dyslipidaemia |
Boosting
Drug | Adverse Effect(s) |
---|---|
RTV |
Nausea and diarrhoea |
COBI | Nausea and diarrhoea ↓ eGFR(iii) Dyslipidaemia |
INSTI
Drug | Adverse Effect(s) |
---|---|
DTG |
Rash |
BIC |
↓ eGFR(iii) |
CAB |
Injection site reactions(vi) |
EVG/c |
Nausea |
RAL | Nausea Myopathy Rhabdomyolysis Sleep disturbance Headache Weight gain Systemic hypersensitivity syndrome(viii) |
Entry inhibitors
Drug | Adverse Effect(s) |
---|---|
LEN |
Injection site reactions |
MVC | Hepatitis Postural hypotension |
Ibalizumab |
Rash |
FTR |
Rash |
ENF |
Injection site reactions |
- TDF and TAF are prodrugs of tenofovir. TDF, but not TAF, may have kidney and bone toxicity particularly when co-administered with RTV or COBI boosting. TDF, but not TAF, decreases plasma lipids. TAF, but not TDF, may promote weight gain particularly when co-administered with DTG or BIC, see Bone Disease: Screening and Diagnosis, Kidney Disease: Definition, Diagnosis and Management, ARV-associated Nephrotoxicity, Weight gain and Obesity
- Still available, but generally not recommended due to toxicity
- Due to inhibition of renal tubular creatinine secretion without affecting glomerular filtration itself
- ATV can be used unboosted or boosted with low-dose RTV or COBI. ATV-related adverse effects are more common with boosting. DRV can be used boosted with low-dose RTV or COBI. Both low-dose RTV and COBI as boosters may cause minor digestive problems and lipid increases (low-dose RTV more than COBI). Coronary heart disease reported with ritonavir-boosted DRV only (no data with COBI-boosted DRV, although lipid effects lower)
- Frequency and severity differs between individual PIs
- CAB is available in oral or injectable formulations; injection site reactions are an adverse effect of injectable CAB
- Pyrexia includes feeling hot or body temperature increased
- DRESS syndrome reported in a few cases, potentially associated to HLA-B*53
* Refers to effects seen in relation to hypersensitivity reactions
Notes:
- The adverse effects listed in the table above are not exhaustive, but represent the most important effects with a likely causal relation. Nausea, diarrhoea and rash are frequently observed in persons on ART, and these symptoms are indicated in the table for drugs where clinical experience suggests a possible causal link
- D4T, ddI, FPV, IDV, SQV and TPR removed. Please refer to EACS v9.1 for details, http://www.eacsociety.org/files/2018_guidelines-9.1-english.pdf