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. 2023 Feb 17;14:1028257. doi: 10.3389/fphar.2023.1028257

TABLE 6.

Summary of adverse drug events.

Type of interventions Number of RCTs Groups Total sample size Incidence Detailed ADR events (number of cases)
PGE1+SMI vs. PGE1 0 PGE1+SMI 0
PGE1 0
PGE1+DCI vs. PGE1 1 PGE1+DCI 65 3.08% Anorexia (1), constipation(1)
PGE1 65 4.62% Diarrhea (1), Dizziness(1), Fever(1)
PGE1+DHI vs. PGE1 4 PGE1+DHI 147 0.00% None
PGE1 144 0.00% None
PGE1+HQI vs. PGE1 5 PGE1+HQI 433 16.86% Dizziness (19), headache (17), pain at the injection site (36), allergies (1)
PGE1 415 14.70% Dizziness (24), pain at the injection site (27), redness at the injection site (4), vomiting (5), diarrhea (1),
PGE1+SKI vs. PGE1 4 PGE1+SKI 136 0.74% Pain and flushing at the injection site (1)
PGE1 116 0.00% None
PGE1+SXTI vs. PGE1 2 PGE1+SXTI 96 0.00% None
PGE1 90 0.00% None
PGE1+XBJI vs. PGE1 1 PGE1+XBJI 30 0.00% None
PGE1 30 0.00% None

SMI, Salvia miltiorrhiza injection; DCI, Danshen-Chuanxiongqin injection; DHI, Danhong injection; HQI, Huangqi injection; SKI, Shenkang injection; SXTI, Shuxuetong injection; XBJI, Xuebijing injection; PGE1, alprostadil injection.