600 IU and 1200 IU: The most frequently reported adverse drug reactions (ADR) during treatment with MENOPUR in clinical trials are Ovarian Hyperstimulation Syndrome, OHSS, headache, abdominal pain, abdominal distension and injection site pain.
None of these ADRs have been reported with an incidence rate of more than 5%.
The table as follows displays the main ADRs in women treated with MENOPUR in clinical trials distributed by system organ classes (SOCs) and frequency. Further, the ADRs seen during post-marketing experience are mentioned with unknown frequency.
75 IU: (See Table 1.)

600 IU and 1200 IU: (See Table 2.)

View ADR Reporting Link