The 1864 preparations contain either crude opium or its aqueous Extractum Opii; those quantities must be distinguished from a quantity of isolated morphine. The following are the officinal opium preparations. Ratios for solids mean the mass fraction in the compounded preparation; liquid strengths specify mass per volume or the actual ingredients used.
- Emplastrum Opii: powdered opium in resin plaster: 1 in 10.
- Enema Opii: opium tincture 30 minims with starch decoction 2 fluid ounces. Thus the tincture is 1 volume to 32 volumes of vehicle, before mixing.
- Extractum Opii: aqueous solvent extraction of 1 avoirdupois pound of sliced opium with 6 Imperial pints of distilled water, in three successive portions, followed by evaporation. The prescribed starting quantities do not impose a fixed yield or a universal crude-drug-to-extract potency ratio.
- Extractum Opii Liquidum: Extractum Opii 1 avoirdupois ounce, distilled water 17 fluid ounces, rectified spirit 3 fluid ounces: 1 ounce of extract to the pint of liquid ingredients.
- Linimentum Opii: equal volumes of opium tincture and soap liniment: half the tincture's nominal opium strength.
- Pilula Opii: powdered opium with hard soap: 1 in 5 of the nominal pill ingredients.
- Pilula Plumbi cum Opio: powdered opium with lead acetate and confection of roses: 1 in 8.
- Pulvis Cretae Aromaticus cum Opio: powdered opium with aromatic chalk powder: 1 in 40.
- Pulvis Ipecacuanhae cum Opio: powdered opium with ipecacuanha and potassium sulfate: 1 in 10.
- Pulvis Kino cum Opio: powdered opium with kino and cinnamon: 1 in 20.
[ref]
The Essentials of Materia Medica and Therapeutics by Alfred Baring Garrod (1865). Papaverceae, part 2, British formulas outside the bracketed American additions; underlying revision dated May 1864
- Tinctura Camphorae cum Opio: opium 40 grains to 1 Imperial pint of proof spirit, with benzoic acid, camphor and anise oil: 2 grains of opium per fluid ounce.
- Opium tincture, Tinctura Opii: powdered opium 1½ avoirdupois ounces to 1 Imperial pint of proof spirit. Nominally this is 32.8125 grains per fluid ounce, or approximately 1 grain per 14.63 minims.
- Trochisci Opii: 72 grains of Extractum Opii in 720 lozenges: one tenth of a grain of extract per lozenge.
- Unguentum Gallae cum Opio: powdered opium 32 grains added to 1 avoirdupois ounce of gall ointment. The actual nominal total is grains, giving 32/469.5 by mass, approximately 1 in 14.67; “32 grains to the ounce of ointment taken” is not 32 grains per final ounce.
- Vinum Opii: powdered opium 1½ avoirdupois ounces, sherry 1 Imperial pint: the tincture's nominal opium proportion, in a different solvent. This formula uses crude opium, not Extractum Opii.
[ref]
The Essentials of Materia Medica and Therapeutics by Alfred Baring Garrod (1865). Papaverceae, part 3, British tincture, lozenge, ointment and wine formulas
The arithmetic uses the new avoirdupois ounce of 437.5 grains, not the old apothecaries' ounce of 480 grains. These are historical formulation proportions, not modern assays of morphine delivered after solvent extraction. Confectio Opii was omitted in 1864, and this edition's Vinum Opii contains no spices. The separate morphine hydrochloride preparations—Liquor Morphiae Hydrochloratis, Suppositoria Morphiae, Trochisci Morphiae, and Trochisci Morphiae et Ipecacuanhae—contain an isolated alkaloid salt rather than crude opium. [ref]
The Prescriber's Analysis of the British Pharmacopoeia by John Birkbeck Nevins (1864). pp. 11–12, 39 and 75–76
Ordinary air contains water vapour, carbon dioxide, variable trace gases and suspended particles in addition to nitrogen and oxygen. Which traces are detected depends on location, sampling volume and test sensitivity. A negative small-sample test is not proof of complete absence.
Water vapour is shown by condensation on a sufficiently cold surface or by the colour change of a suitable dry indicator: white anhydrous copper(II) sulfate becomes blue on hydration. Passing a known air stream through a drying tube and observing a controlled mass increase gives a more quantitative principle, provided other absorbable vapours are excluded.
Carbon dioxide gives a calcium carbonate turbidity when a suitable air sample is passed into clear limewater:Large excess of carbon dioxide can redissolve the deposit as dissolved bicarbonate species, so excessive exposure can obscure the initial result. Absorption into an alkaline solution, followed by an appropriate carbonate test, concentrates the trace component.
Ammonia and ammonium-bearing particles may be collected by an acid wash and examined after suitable neutralization or liberation of the Ammonia. Nessler's reagent supplies a sensitive colour test, with a blank to exclude contaminated reagents. Simple moist litmus is much less sensitive. Acidic gases and nitrogen oxides may instead be collected in appropriate wash solutions and examined with tests for the resulting anions; their identity cannot be inferred from acidity alone.
Near relevant sources, hydrogen sulfide can blacken moist lead acetate paper by forming lead sulfide. Ozone-sensitive starch–iodide paper can indicate an oxidizing trace constituent through liberation of iodine, but other oxidants can give the same response: the historical observation is not a specific proof of ozone. Dust and droplets can be collected on a filter or surface and examined by microscopy, with chemical tests applied to separated material as needed.
Modern analysis also recognizes argon and other noble gases, as well as many low-concentration pollutants, using instrumental separation and spectroscopy. Their modern recognition should not be silently included among discoveries available to an 1865 candidate. The useful answer pairs each proposed constituent with a collection method, a specific reaction or observation, and the limits of that test.
Severe haemoptysis in a person described historically as “phthisical” requires immediate attention to breathing and circulatory danger; the treatment of chronic wasting cannot wait in place of control of the acute bleeding. The historical label suggests pulmonary tuberculosis, but does not itself prove that diagnosis or identify the bleeding vessel.
In period terms, the sensible supportive aims were quiet, reduced exertion and observation of the blood loss and general condition. The intent was to avoid provoking further cough or dislodging a clot, while preserving the person's remaining strength. A depleted person with chronic wasting was a poor candidate for reflex general bloodletting. The historical pharmacological literature included astringents, mineral salts and external cold, but the mere sequence “remedy administered, bleeding stopped” could not establish efficacy: haemoptysis often varied or stopped temporarily on its own.
This uncertainty was recognized before the examination. An 1862 discussion lists astringents such as lead acetate, emetic drugs and external ice among competing treatments, and questions the evidential value of events following their use. It also records opposing fashions of severe dietary restriction and frequent feeding with stimulants.[ref]
On the Treatment of Tubercular Hemoptysis by William Brinton. 1862, pp. 553–557, opening discussion of competing specifics and the limitations of apparent therapeutic success
The same author advocated a digitalis preparation with close pulse observation for severe attacks, hoping to influence the circulation; he emphasized its dangers. This is a period proposal, not modern emergency treatment. The historical explanation is why rest and supposed haemostatic remedies were attempted, not a claim that they reliably closed a ruptured vessel. No toxic nineteenth-century mixture is recommended here.Modern correction: life-threatening haemoptysis is an airway emergency, often killing through obstruction and loss of gas exchange. Its severity depends on respiratory and circulatory effects, not just the estimated volume in a basin. Obtain emergency specialist support, maintain oxygenation and protect the unaffected lung; when the bleeding side is known, positioning that side down can limit contamination of the other side. Secure suitable intravenous access, assess haemoglobin and coagulation, prepare for needed blood transfusion and correct important coagulopathy. In unstable ongoing bleeding, securing the airway and bronchoscopy can take precedence over transport for imaging.[ref]
Society of Chest Imaging and Interventions Consensus Guidelines for the Interventional Radiology Management of Hemoptysis. 2023, initial management of life-threatening hemoptysis; airway isolation, positioning and haemodynamic stabilization
Once sufficiently stable, computed tomography angiography helps locate the source and plan treatment. Bronchial artery embolisation is a principal means of controlling severe or recurrent haemoptysis from abnormal systemic vessels. Bronchoscopy can assist localization and temporary control; selected lesions or failed endovascular control may require surgery. Do not assume every tuberculosis-associated haemorrhage comes from the same vascular bed. The intervention must match the demonstrated source. Modern management also treats the underlying disease; stopping bleeding alone does not cure pulmonary tuberculosis.[ref]
CIRSE Standards of Practice on Bronchial Artery Embolisation. 2022, Table 1; indications; diagnostic and treatment pathways
Suspected active pulmonary tuberculosis warrants appropriate respiratory infection-control measures, diagnostic sampling when safe and a susceptibility-informed multidrug antibiotic regimen once the diagnosis and treatment plan are established.[ref]Treatment for Drug-Susceptible Tuberculosis Disease by CDC. Choice of regimen; drug susceptibility, coexisting conditions and interactions
Quiet surroundings can still help, but neither ice nor a historical astringent substitutes for these measures.