Drug intelligence / Profile preview

drotaverine + ibuprofen

Development stage
Discontinued
Lead developer
Sanofi
Modality
Small Molecules
Administration
Oral
01

Overview

A fixed-dose combination drug containing **drotaverine**, an antispasmodic agent (phosphodiesterase 4 inhibitor), and **ibuprofen**, a nonsteroidal anti-inflammatory drug (NSAID) with analgesic and anti-inflammatory action. The combination is formulated to provide both relief from smooth muscle spasms and pain, particularly effective in conditions such as menstrual cramps (dysmenorrhea) and abdominal spasms. Drotaverine acts by selectively inhibiting phosphodiesterase 4 (PDE4), relaxing smooth muscle without anticholinergic effects, while ibuprofen inhibits cyclooxygenase (COX) enzymes to decrease prostaglandin synthesis, reducing inflammation and pain[1][3][4]. The combination may be available as a monolithic or bilayer tablet developed for improved patient compliance and enhanced efficacy in pain management[4].

Brand names
Algoflex-M
Other names
drotaverine hydrochloride + ibuprofen
02

Targets

PGHS-1 (Prostaglandin G/H Synthase 1)PTGS2 (Prostaglandin-Endoperoxide Synthase 2)CACNA1C (Voltage-dependent L-type calcium channel subunit alpha-1C)PDE4 (Phosphodiesterase 4A1)

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