F
KAB; UPW); Hypotensive (1; WOI); Insecticide (1; UPW); Lipogenic (fl; UPW); Pectoral (f;
KAB); Protisticide (1; WOI); Sedative (f; KAP); Stomachic (f; KAP); Teratogen (1; ZUL); Tonic
(f; DEP; HHB; KAB; MBB; WOI).Indications (Flannelweed) — Ameba (1; HDN; WOI); Angina (f; MBB); Arthrosis (f; MBB);
Asthma (1; KAP; UPW); Biliousness (f; WOI); Bleeding (f; KAB; KAP); Bronchosis (1; MBB;
UPW); Cardiopathy (f; MBB); Caries (1; HDN); Circulosis (f; MBB); Colic (f; DEP; KAB;
WOI); Conjunctivosis (f; UPW); Convulsion (1; HDN); Cough (f; KAB); Cystosis (f; WOI);
Diarrhea (f; HDN; UPW); Dysentery (f; UPW; WOI); Dysuria (f; KAB; KAP); Elephantiasis
(f; KAP; WOI); Fever (1; HDN; KAB; KAP; WOI); Fungus (f; KAB); Gonorrhea (f; HHB;
KAB; KAP; WOI); Hay Fever (1; UPW); Hematuria (f; WOI); Hemiplegia (f; DEP; WOI);
Hemorrhoid (f; KAB; KAP; WOI); High Blood Pressure (1; WOI); Inflammation (f; KAB);
Insanity (f; KAB; KAP); Insomnia (f; KAP); Leukorrhea (f; DEP; KAB; WOI); Low Blood
Pressure (1; UPW); Lumbago (f; HDN); Malaria (f; DEP; HHB; KAB); Migraine (1; UPW);
Myosis (f; MBB); Nervousness (f; KAP); Neurosis (f; KAB); Ophthalmia (f; KAB; UPW);
Paralysis (f; DEP; KAB; KAP; WOI); Phthisis (f; KAB); Pneumonia (f; HDN); Polyuria (f;
DEP; KAB; WOI); Pulmonosis (f; HDN); Rheumatism (f; HDN; KAP); Ringworm (f; KAB);
Sciatica (f; KAB; WOI); Snakebite (f; UPW); Sore (f; WOI); Spermatorrhea (f; KAB); Spondy-
losis (f; MBB); Sprain (f; UPW); Strangury (f; WOI); Swelling (f; UPW); Syphilis (f; HDN);
Tenesmus (f; DEP; KAB; WOI); Throat (f; KAB); VD (f; KAB); Tuberculosis (f; MBB); Water
Retention (f; WOI); Worm (f; UPW); Wound (f; KAB).Dosages (Flannelweed) — 1–3 g powder (KAP); 2–20 ml root tea (KAP).Extracts (Flannelweed) — HDN presents new pharmacological data; some of it conflicts with
what I provide. For example, in HDN, vasicinone was reported as a bronchoconstrictor in vivo
and as a bronchodilator in vitro. HDN gives us the activities for L-ephedrine, while not specifically
naming it in the plant. Beta-phenylethylamine is the parent of many different sympathomimetic
phytochemicals. Well absorbed, it easily crosses the blood-brain barrier, decreasing amine content
in noradrenalin and dopamine-containing nerve terminals in the brain and in the peripheral
adrenergic nerve terminals of rats (HDN). Its amphetamine-like action can be blocked by
pretreatment with reserpine (HDN).