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The same increase in relative risk was seen in women ? 49 and in women ? 50, although fewer events occurred in younger women. Women with thromboembolic events were at risk for a second related event (7 out of 25 women on placebo, 5 out of 48 women on Nolvadex) and were at risk for complications of the event and its treatment (0/25 on placebo, 4/48 on Nolvadex). Among women receiving Nolvadex, deep vein thrombosis events occurred between 2 and 57 months (average=19 months) from the start of treatment. There was a non-statistically significant increase in stroke among patients randomized to Nolvadex (24-Placebo; 34-Nolvadex; RR=1. Six of the 24 strokes in the placebo group were considered hemorrhagic in origin and 10 of the 34 strokes in the Nolvadex group were categorized as hemorrhagic. Seventeen of the 34 strokes in the Nolvadex group were considered occlusive and 7 were considered to be of unknown etiology. 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