DRUG HYPERSENSITIVITY | 173 |
DRUG INEFFECTIVE | 64 |
OFF LABEL USE | 59 |
HYPERSENSITIVITY | 57 |
RENAL FAILURE ACUTE | 54 |
DYSPNOEA | 54 |
DRUG INTERACTION | 54 |
NAUSEA | 52 |
ANAPHYLACTIC REACTION | 49 |
Acute kidney injury | 47 |
VOMITING | 42 |
URTICARIA | 39 |
PRURITUS | 33 |
RASH | 32 |
HYPOTENSION | 32 |
HAEMORRHAGE | 31 |
NASAL DISCOMFORT | 30 |
ULCERATIVE KERATITIS | 29 |
Incorrect drug administration duration | 29 |
EYE IRRITATION | 28 |
ERYTHEMA | 28 |
EYE PAIN | 27 |
GASTRIC ULCER | 25 |
MEDICATION ERROR | 23 |
ANGIOEDEMA | 21 |
TACHYCARDIA | 20 |
MELAENA | 20 |
GASTROINTESTINAL HAEMORRHAGE | 20 |
DIZZINESS | 20 |
CHEST PAIN | 20 |
BLOOD CREATININE INCREASED | 20 |
ASTHMA | 20 |
ABDOMINAL PAIN UPPER | 20 |
VISION BLURRED | 19 |
Product use issue | 19 |
DRUG PRESCRIBING ERROR | 19 |
DEATH | 19 |
ABDOMINAL PAIN | 19 |
PYREXIA | 17 |
INJECTION SITE PAIN | 17 |
PAIN | 16 |
HEADACHE | 16 |
BURNING SENSATION | 16 |
OCULAR HYPERAEMIA | 15 |
HAEMATEMESIS | 15 |
GASTRITIS EROSIVE | 15 |
Product use in unapproved indication | 14 |
Lip oedema | 14 |
DRUG ADMINISTRATION ERROR | 14 |
Contraindicated product administered | 14 |
WHEEZING | 13 |
THROAT TIGHTNESS | 13 |
TACHYPNOEA | 13 |
RENAL FAILURE | 13 |
PRODUCT QUALITY ISSUE | 13 |
FACE OEDEMA | 13 |
DUODENAL ULCER | 13 |
CARDIO-RESPIRATORY ARREST | 13 |
ANAEMIA | 13 |
VISUAL IMPAIRMENT | 12 |
VISUAL ACUITY REDUCED | 12 |
HAEMOGLOBIN DECREASED | 12 |
EYELID OEDEMA | 12 |
CONFUSIONAL STATE | 12 |
BLOOD PRESSURE INCREASED | 12 |
SYNCOPE | 11 |
RENAL TUBULAR NECROSIS | 11 |
RENAL IMPAIRMENT | 11 |
MALAISE | 11 |
KERATITIS | 11 |
FEELING ABNORMAL | 11 |
CONDITION AGGRAVATED | 11 |
CARDIAC ARREST | 11 |
SWELLING FACE | 10 |
RHABDOMYOLYSIS | 10 |
POST PROCEDURAL HAEMORRHAGE | 10 |
LOSS OF CONSCIOUSNESS | 10 |
Labelled drug-drug interaction medication error | 10 |
INJECTION SITE ERYTHEMA | 10 |
HYPERHIDROSIS | 10 |
Drug abuse | 10 |
DISSEMINATED INTRAVASCULAR COAGULATION | 10 |
DIARRHOEA | 10 |
CORNEAL OEDEMA | 10 |
CHEST DISCOMFORT | 10 |
ASTHENIA | 10 |
Wrong technique in product usage process | 9 |
WEIGHT INCREASED | 9 |
TREMOR | 9 |
Spinal epidural haematoma | 9 |
Retinal pigment epitheliopathy | 9 |
PURPURA FULMINANS | 9 |
PHARYNGEAL OEDEMA | 9 |
OVERDOSE | 9 |
OEDEMA PERIPHERAL | 9 |
Extradural haematoma | 9 |
EPISTAXIS | 9 |
ENDOPHTHALMITIS | 9 |
BRONCHOSPASM | 9 |
BRADYCARDIA | 9 |
BACK PAIN | 9 |
SWOLLEN TONGUE | 8 |
SOMNOLENCE | 8 |
RESPIRATORY FAILURE | 8 |
RESPIRATORY DISTRESS | 8 |
NEPHROLITHIASIS | 8 |
METABOLIC ACIDOSIS | 8 |
INCORRECT DOSE ADMINISTERED | 8 |
EYE SWELLING | 8 |
CORNEAL DISORDER | 8 |
ANAPHYLACTIC SHOCK | 8 |
Treatment failure | 7 |
Throat irritation | 7 |
Quadriplegia | 7 |
PUNCTATE KERATITIS | 7 |
Pulmonary alveolar haemorrhage | 7 |
Product container issue | 7 |
POST PROCEDURAL COMPLICATION | 7 |
PALPITATIONS | 7 |
PAIN IN EXTREMITY | 7 |
OXYGEN SATURATION DECREASED | 7 |
OEDEMA | 7 |
NECROTISING FASCIITIS | 7 |
INTRAOCULAR PRESSURE INCREASED | 7 |
HYPOAESTHESIA | 7 |
GASTRITIS | 7 |
FLUSHING | 7 |
FATIGUE | 7 |
EROSIVE DUODENITIS | 7 |
Drug administered to patient of inappropriate age | 7 |
DIALYSIS | 7 |
COMPLETED SUICIDE | 7 |
COMA | 7 |
ANURIA | 7 |
ABDOMINAL DISTENSION | 7 |
Urine output decreased | 6 |
UNRESPONSIVE TO STIMULI | 6 |
Toxic anterior segment syndrome | 6 |
RECTAL HAEMORRHAGE | 6 |
PROTHROMBIN TIME PROLONGED | 6 |
Product administration error | 6 |
NO ADVERSE EVENT | 6 |
MUSCLE SPASMS | 6 |
HALLUCINATION, VISUAL | 6 |
HAEMATOCRIT DECREASED | 6 |
GASTRIC HAEMORRHAGE | 6 |
Dysphagia | 6 |
Discomfort | 6 |
CORNEAL THINNING | 6 |
CHILLS | 6 |
BLOOD BILIRUBIN INCREASED | 6 |
Weight decreased | 5 |
UNDERDOSE | 5 |
Toxicity to various agents | 5 |
THROMBOCYTOPENIA | 5 |
STEVENS-JOHNSON SYNDROME | 5 |
Sensory loss | 5 |
Rhinorrhoea | 5 |
RETROPERITONEAL HAEMORRHAGE | 5 |
Renal infarct | 5 |
RASH GENERALISED | 5 |
PRODUCT LABEL ISSUE | 5 |
Product dispensing error | 5 |
Pneumonia | 5 |
OLIGURIA | 5 |
MUSCULAR WEAKNESS | 5 |
INFLAMMATION | 5 |
INCORRECT ROUTE OF DRUG ADMINISTRATION | 5 |
HYPOXIA | 5 |
HEPATIC FUNCTION ABNORMAL | 5 |
FOREIGN BODY SENSATION IN EYES | 5 |
FEELING HOT | 5 |
EYE INFLAMMATION | 5 |
EYE DISORDER | 5 |
Expired product administered | 5 |
DECREASED APPETITE | 5 |
COUGH | 5 |
CORNEAL SCAR | 5 |
CONVULSION | 5 |
CHROMATURIA | 5 |
CEREBRAL HAEMORRHAGE | 5 |
BLOOD UREA INCREASED | 5 |
BLOOD ALKALINE PHOSPHATASE INCREASED | 5 |
BLISTER | 5 |
ARTHRALGIA | 5 |
AGRANULOCYTOSIS | 5 |
AGITATION | 5 |
ACUTE RESPIRATORY FAILURE | 5 |
UPPER GASTROINTESTINAL HAEMORRHAGE | 4 |
Toxic epidermal necrolysis | 4 |
Tongue oedema | 4 |
Swelling | 4 |
Sneezing | 4 |
Skin plaque | 4 |
SKIN EXFOLIATION | 4 |
SEPTIC SHOCK | 4 |
SEPSIS | 4 |
Seizure | 4 |
Sedation | 4 |
Retching | 4 |
Renal ischaemia | 4 |
PULMONARY OEDEMA | 4 |
Product prescribing error | 4 |
Product label confusion | 4 |
PARAESTHESIA | 4 |
PALLOR | 4 |
Nasal disorder | 4 |
Myalgia | 4 |
MUSCLE TWITCHING | 4 |
LIP SWELLING | 4 |
LACRIMATION INCREASED | 4 |
JOINT SWELLING | 4 |
International normalised ratio increased | 4 |
INJECTION SITE SWELLING | 4 |
Hyponatraemia | 4 |
HYPERTENSION | 4 |
HYPERKALAEMIA | 4 |
Hydronephrosis | 4 |
Haemorrhage intracranial | 4 |
HAEMATURIA | 4 |
GENERALISED ERYTHEMA | 4 |
GENERAL PHYSICAL HEALTH DETERIORATION | 4 |
FALL | 4 |
EYE PRURITUS | 4 |
DYSTONIA | 4 |
DUODENAL ULCER PERFORATION | 4 |
DUODENAL ULCER HAEMORRHAGE | 4 |
DEHYDRATION | 4 |
CORNEAL PERFORATION | 4 |
Corneal abrasion | 4 |
CONTUSION | 4 |
COLD SWEAT | 4 |
BLINDNESS | 4 |
ANXIETY | 4 |
ADVERSE DRUG REACTION | 4 |
ABDOMINAL DISCOMFORT | 4 |
Wrong product administered | 3 |
WOUND DEHISCENCE | 3 |
VERTIGO | 3 |
VENTRICULAR TACHYCARDIA | 3 |
VENTRICULAR FIBRILLATION | 3 |
URINARY INCONTINENCE | 3 |
THROMBOSIS | 3 |
SOPOR | 3 |
SKIN DISCOLOURATION | 3 |
Sinusitis | 3 |
SINUS TACHYCARDIA | 3 |
Salivary hypersecretion | 3 |
Respiratory depression | 3 |
RESPIRATORY ARREST | 3 |
RENAL FAILURE CHRONIC | 3 |
REFUSAL OF TREATMENT BY PATIENT | 3 |
Recalled product administered | 3 |
RASH PRURITIC | 3 |
Rash maculo-papular | 3 |
RASH ERYTHEMATOUS | 3 |
Pulmonary function test decreased | 3 |
Procedural pain | 3 |
Presyncope | 3 |
POLYURIA | 3 |
Polyneuropathy | 3 |
Peripheral swelling | 3 |
Periorbital swelling | 3 |
Periorbital oedema | 3 |
NO THERAPEUTIC RESPONSE | 3 |
MENTAL STATUS CHANGES | 3 |
MACULAR OEDEMA | 3 |
Kounis syndrome | 3 |
Interstitial lung disease | 3 |
INJECTION SITE REACTION | 3 |
Incorrect product storage | 3 |
Inappropriate schedule of product administration | 3 |
HYPOPYON | 3 |
Hypertensive crisis | 3 |
Hyperpyrexia | 3 |
Hyperglycaemia | 3 |
Heart rate increased | 3 |
Hallucination | 3 |
HAEMORRHAGIC ANAEMIA | 3 |
Haemoptysis | 3 |
HAEMATOCHEZIA | 3 |
GOUT | 3 |
GENERALISED OEDEMA | 3 |
GASTROINTESTINAL DISORDER | 3 |
GASTRIC ULCER HAEMORRHAGE | 3 |
Forced expiratory volume decreased | 3 |
EYE DISCHARGE | 3 |
Dyskinesia | 3 |
DYSARTHRIA | 3 |
DUODENITIS | 3 |
Dry eye | 3 |
DIPLOPIA | 3 |
CRYING | 3 |
CORNEAL ULCER | 3 |
CORNEAL OPACITY | 3 |
CORNEAL EPITHELIUM DEFECT | 3 |
Corneal dystrophy | 3 |
Contraindicated drug prescribed | 3 |
Constipation | 3 |
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR | 3 |
CARDIAC DISORDER | 3 |
BLOOD PRESSURE DECREASED | 3 |
BALANCE DISORDER | 3 |
ASPARTATE AMINOTRANSFERASE INCREASED | 3 |
ARRHYTHMIA | 3 |
Aphthous ulcer | 3 |
APHASIA | 3 |
ANGIONEUROTIC OEDEMA | 3 |
ANGINA PECTORIS | 3 |
ALANINE AMINOTRANSFERASE INCREASED | 3 |
Acidosis | 3 |
WRONG TECHNIQUE IN DRUG USAGE PROCESS | 2 |
Vulvovaginal discomfort | 2 |
Vitreous floaters | 2 |
Ventricular extrasystoles | 2 |
VARICES OESOPHAGEAL | 2 |
UNEVALUABLE EVENT | 2 |
Tubulointerstitial nephritis | 2 |
TREATMENT NONCOMPLIANCE | 2 |
Transaminases increased | 2 |
Toxic skin eruption | 2 |
Thrombophlebitis | 2 |
Therapy non-responder | 2 |
SUPERFICIAL INJURY OF EYE | 2 |
SUICIDE ATTEMPT | 2 |
Status epilepticus | 2 |
Spinal column stenosis | 2 |
SKIN TOXICITY | 2 |
SKIN BURNING SENSATION | 2 |
Shock haemorrhagic | 2 |
ROAD TRAFFIC ACCIDENT | 2 |
RESPIRATORY RATE DECREASED | 2 |
RESPIRATORY DISORDER | 2 |
Respiratory acidosis | 2 |
Renal tubular injury | 2 |
Rash papular | 2 |
RASH MACULAR | 2 |
Pyelonephritis | 2 |
PULMONARY HAEMORRHAGE | 2 |
PULMONARY EMBOLISM | 2 |
PRURITUS GENERALISED | 2 |
PRODUCT SUBSTITUTION ISSUE | 2 |
Product storage error | 2 |
Product preparation issue | 2 |
Product preparation error | 2 |
Product packaging quantity issue | 2 |
Product packaging confusion | 2 |
Product dropper issue | 2 |
Product dose omission issue | 2 |
Product dose omission | 2 |
Product complaint | 2 |
PROCEDURAL HYPOTENSION | 2 |
Prescription drug used without a prescription | 2 |
Prerenal failure | 2 |
POST PROCEDURAL HAEMATOMA | 2 |
PHOTOPHOBIA | 2 |
Pharyngeal swelling | 2 |
PETECHIAE | 2 |
PERITONITIS | 2 |
PERICARDITIS | 2 |
Paraplegia | 2 |
ORTHOSTATIC HYPOTENSION | 2 |
OESOPHAGITIS | 2 |
NEUTROPENIA | 2 |
Neurotoxicity | 2 |
Nephropathy toxic | 2 |
NEPHRITIS INTERSTITIAL | 2 |
Necrotising oesophagitis | 2 |
NECK PAIN | 2 |
Myocardial infarction | 2 |
Multiple organ dysfunction syndrome | 2 |
MOTOR DYSFUNCTION | 2 |
Mixed liver injury | 2 |
Migraine | 2 |
MALLORY-WEISS SYNDROME | 2 |
LUNG DISORDER | 2 |
LARYNGEAL OEDEMA | 2 |
LACERATION | 2 |
Keratopathy | 2 |
JAUNDICE | 2 |
Ischaemia | 2 |
INTRA-ABDOMINAL HAEMORRHAGE | 2 |
INTESTINAL OBSTRUCTION | 2 |
Intercepted drug prescribing error | 2 |
INTENTIONAL OVERDOSE | 2 |
INSOMNIA | 2 |
INJECTION SITE RASH | 2 |
INFUSION SITE PAIN | 2 |
Influenza | 2 |
Incorrect route of product administration | 2 |
Impaired healing | 2 |
ILL-DEFINED DISORDER | 2 |
Ileus paralytic | 2 |
Hypothermia | 2 |
HYPOPHAGIA | 2 |
Hypomagnesaemia | 2 |
Hypokinesia | 2 |
Hypokalaemia | 2 |
Hypocalcaemia | 2 |
HYPOAESTHESIA ORAL | 2 |
HYPERAESTHESIA | 2 |
HIP FRACTURE | 2 |
Hepatitis cholestatic | 2 |
HEPATIC ENZYME INCREASED | 2 |
Hemianopia homonymous | 2 |
Haematoma | 2 |
HAEMARTHROSIS | 2 |
Gastrooesophageal reflux disease | 2 |
Gastroduodenal ulcer | 2 |
Gastric perforation | 2 |
Gangrene | 2 |
Flank pain | 2 |
FAECES PALE | 2 |
FAECES DISCOLOURED | 2 |
FAECAL INCONTINENCE | 2 |
EYE INFECTION | 2 |
Eye haemorrhage | 2 |
EXTRAPYRAMIDAL DISORDER | 2 |
Extra dose administered | 2 |
Exposure during pregnancy | 2 |
Escherichia infection | 2 |
EROSIVE OESOPHAGITIS | 2 |
Embolia cutis medicamentosa | 2 |
Ear discomfort | 2 |
DYSPHONIA | 2 |
Dry skin | 2 |
DRUG-INDUCED LIVER INJURY | 2 |
Drug level increased | 2 |
DRUG INTOLERANCE | 2 |
Drug ineffective for unapproved indication | 2 |
Drug effect incomplete | 2 |
Disorientation | 2 |
Dermatitis bullous | 2 |
Cystoid macular oedema | 2 |
Cystocele | 2 |
Cross sensitivity reaction | 2 |
CORNEAL REFLEX DECREASED | 2 |
CORNEAL INFILTRATES | 2 |
CORNEAL EROSION | 2 |
Conjunctivitis | 2 |
COLITIS ISCHAEMIC | 2 |
COGNITIVE DISORDER | 2 |
CEREBROVASCULAR ACCIDENT | 2 |
CELLULITIS | 2 |
Cataract | 2 |
CARDIAC FAILURE CONGESTIVE | 2 |
BRONCHITIS | 2 |
Breast pain | 2 |
BRAIN OEDEMA | 2 |
BRAIN INJURY | 2 |
Bradyphrenia | 2 |
BLOOD URINE PRESENT | 2 |
BLOOD GLUCOSE DECREASED | 2 |
BLOOD CREATINE PHOSPHOKINASE INCREASED | 2 |
BLOOD CREATINE INCREASED | 2 |
Aspirin-exacerbated respiratory disease | 2 |
Arteriospasm coronary | 2 |
ARTERIOSCLEROSIS | 2 |
Apnoea | 2 |
Antiphospholipid antibodies positive | 2 |
Anterior chamber inflammation | 2 |
ANTERIOR CHAMBER CELL | 2 |
ACTIVITIES OF DAILY LIVING IMPAIRED | 2 |
Accidental exposure to product | 2 |
ABDOMINAL PAIN LOWER | 2 |
Wrong schedule | 1 |
Wrong product stored | 1 |
Wrong patient received medication | 1 |
Wrong drug administered | 1 |
Wound secretion | 1 |
Wound | 1 |
WHITE CLOT SYNDROME | 1 |
WHEELCHAIR USER | 1 |
Weight bearing difficulty | 1 |
VON WILLEBRAND'S FACTOR MULTIMERS ABNORMAL | 1 |
VITRITIS | 1 |
Vitreous opacities | 1 |
Visual field defect | 1 |
Ventricular arrhythmia | 1 |
Venous thrombosis limb | 1 |
VASOCONSTRICTION | 1 |
VASCULAR ACCESS COMPLICATION | 1 |
VAGINAL HAEMORRHAGE | 1 |
VAGINAL DISORDER | 1 |
Uveitis | 1 |
Urinary retention | 1 |
UPPER RESPIRATORY TRACT INFECTION | 1 |
TROPONIN INCREASED | 1 |
Transient ischaemic attack | 1 |
Torsade de pointes | 1 |
THIRST | 1 |
Therapy partial responder | 1 |
Therapeutic response unexpected | 1 |
Therapeutic response decreased | 1 |
Therapeutic product effect increased | 1 |
TERMINAL INSOMNIA | 1 |
Tenderness | 1 |
Tearfulness | 1 |
Symptom masked | 1 |
Suspected suicide | 1 |
Suspected product contamination | 1 |
Supraventricular tachycardia | 1 |
SUICIDAL IDEATION | 1 |
SUFFOCATION FEELING | 1 |
SUDDEN ONSET OF SLEEP | 1 |
Sudden cardiac death | 1 |
SUBCLAVIAN VEIN THROMBOSIS | 1 |
Subcapsular hepatic haematoma | 1 |
STUPOR | 1 |
STRIDOR | 1 |
Stress cardiomyopathy | 1 |
Streptococcus test positive | 1 |
Streptococcal infection | 1 |
Strabismus | 1 |
Staphylococcal sepsis | 1 |
SPUTUM DISCOLOURED | 1 |
SPUTUM ABNORMAL | 1 |
Spontaneous haematoma | 1 |
SPLEEN CONGESTION | 1 |
Spinal subdural haematoma | 1 |
Spinal cord haematoma | 1 |
SPEECH DISORDER | 1 |
Soft tissue necrosis | 1 |
Soft tissue inflammation | 1 |
Soft tissue haemorrhage | 1 |
Sleep disorder | 1 |
Skin wrinkling | 1 |
Skin odour abnormal | 1 |
SKIN NECROSIS | 1 |
SKIN IRRITATION | 1 |
Skin haemorrhage | 1 |
Sinus headache | 1 |
Septic embolus | 1 |
SENSE OF OPPRESSION | 1 |
SENSATION OF FOREIGN BODY | 1 |
Self-medication | 1 |
SECRETION DISCHARGE | 1 |
Scratch | 1 |
Scab | 1 |
SARS-CoV-2 test positive | 1 |
RETROPERITONEAL FIBROSIS | 1 |
Retroperitoneal abscess | 1 |
Retinal drusen | 1 |
RESPIRATORY RATE INCREASED | 1 |
Renal papillary necrosis | 1 |
Renal injury | 1 |
RENAL HAEMORRHAGE | 1 |
Renal haematoma | 1 |
RENAL CORTICAL NECROSIS | 1 |
RENAL ARTERY STENOSIS | 1 |
Rash pustular | 1 |
PYOMYOSITIS | 1 |
PURPURA | 1 |
Pulseless electrical activity | 1 |
Pulse pressure increased | 1 |
PULSE ABSENT | 1 |
PULMONARY CONGESTION | 1 |
Psoas abscess | 1 |
PSEUDOPHAKIA | 1 |
PROTHROMBIN TIME ABNORMAL | 1 |
PROTEIN URINE PRESENT | 1 |
PROTEIN TOTAL DECREASED | 1 |
Prostatitis | 1 |
PROSTATIC PAIN | 1 |
Product use complaint | 1 |
Product taste abnormal | 1 |
Product physical issue | 1 |
PRODUCT PACKAGING ISSUE | 1 |
Product odour abnormal | 1 |
Product name confusion | 1 |
Product leakage | 1 |
Product distribution issue | 1 |
Product contamination physical | 1 |
Product contamination microbial | 1 |
Product colour issue | 1 |
Product closure removal difficult | 1 |
Product barcode issue | 1 |
Product appearance confusion | 1 |
Product administration interrupted | 1 |
Priapism | 1 |
Prescribed overdose | 1 |
Pregnancy | 1 |
PRE-ECLAMPSIA | 1 |
Postoperative adhesion | 1 |
Post procedural sepsis | 1 |
Polymerase chain reaction positive | 1 |
Pollakiuria | 1 |
Pneumonia staphylococcal | 1 |
PNEUMONIA ASPIRATION | 1 |
Pleural effusion | 1 |
PLEURAL DISORDER | 1 |
PLATELET COUNT DECREASED | 1 |
PITTING OEDEMA | 1 |
Physical product label issue | 1 |
PHOTOSENSITIVITY REACTION | 1 |
Pharyngeal ulceration | 1 |
PHARYNGEAL ERYTHEMA | 1 |
Peritoneal haemorrhage | 1 |
Perirenal haematoma | 1 |
PERICARDIAL EFFUSION | 1 |
Peptic ulcer perforation | 1 |
PELVIC PAIN | 1 |
Pelvic abscess | 1 |
Parotid gland enlargement | 1 |
Paraparesis | 1 |
PARANOIA | 1 |
Paralysis | 1 |
Papule | 1 |
Papilloedema | 1 |
Panophthalmitis | 1 |
PANIC REACTION | 1 |
Panic disorder | 1 |
PANCYTOPENIA | 1 |
Pancreatitis necrotising | 1 |
Palmoplantar keratoderma | 1 |
Palatal oedema | 1 |
Painful respiration | 1 |
OXYGEN SUPPLEMENTATION | 1 |
OXYGEN SATURATION | 1 |
Osteoporosis | 1 |
Osteomyelitis | 1 |
Oropharyngeal pain | 1 |
Oropharyngeal blistering | 1 |
Oral herpes | 1 |
Oral discomfort | 1 |
OPHTHALMOPLEGIC MIGRAINE | 1 |
Ophthalmic herpes simplex | 1 |
OPERATIVE HAEMORRHAGE | 1 |
Oesophageal infection | 1 |
OEDEMA MUCOSAL | 1 |
OEDEMA MOUTH | 1 |
OCULAR ICTERUS | 1 |
Occupational exposure to product | 1 |
Obstruction gastric | 1 |
NEUROPATHY | 1 |
Neuralgia | 1 |
NERVOUS SYSTEM DISORDER | 1 |
NEPHROTIC SYNDROME | 1 |
Nephropathy | 1 |
NEOVASCULARISATION | 1 |
NECROTISING ENTEROCOLITIS NEONATAL | 1 |
NECROSIS | 1 |
NECK INJURY | 1 |
Nasopharyngitis | 1 |
Nasal ulcer | 1 |
Nasal discharge discolouration | 1 |
Nasal crusting | 1 |
Myositis | 1 |
Myelomalacia | 1 |
Musculoskeletal chest pain | 1 |
MUSCLE RIGIDITY | 1 |
Muscle necrosis | 1 |
MUSCLE DISORDER | 1 |
Muscle atrophy | 1 |
MULTIPLE MYELOMA | 1 |
Multiple injuries | 1 |
MULTIPLE DRUG OVERDOSE INTENTIONAL | 1 |
Multi-organ disorder | 1 |
Mouth swelling | 1 |
MOUTH HAEMORRHAGE | 1 |
Mood altered | 1 |
Monocytosis | 1 |
Mitral valve prolapse | 1 |
MITRAL VALVE INCOMPETENCE | 1 |
Microcytic anaemia | 1 |
Metastasis | 1 |
Metal poisoning | 1 |
Mesenteric haemorrhage | 1 |
Mental impairment | 1 |
MENINGITIS ASEPTIC | 1 |
MEDICAL DEVICE COMPLICATION | 1 |
Maternal exposure during pregnancy | 1 |
LUNG INFILTRATION | 1 |
Lower gastrointestinal haemorrhage | 1 |
Long QT syndrome | 1 |
Localised oedema | 1 |
LIVER DISORDER | 1 |
Liquid product physical issue | 1 |
Ligament injury | 1 |
LEUKOPENIA | 1 |
Lethargy | 1 |
Left ventricular dysfunction | 1 |
LARYNGOSPASM | 1 |
Laryngeal disorder | 1 |
LARGE INTESTINE PERFORATION | 1 |
LABORATORY TEST ABNORMAL | 1 |
Labelled drug-disease interaction medication error | 1 |
Joint range of motion decreased | 1 |
ISCHAEMIC HEPATITIS | 1 |
Ischaemic cardiomyopathy | 1 |
Iritis | 1 |
IRIS BOMBE | 1 |
Iridocyclitis | 1 |
IRIDOCELE | 1 |
INTUBATION COMPLICATION | 1 |
INTRAVASCULAR HAEMOLYSIS | 1 |
INTESTINAL PERFORATION | 1 |
INTESTINAL ISCHAEMIA | 1 |
International normalised ratio abnormal | 1 |
INTERMITTENT CLAUDICATION | 1 |
Intercepted product prescribing error | 1 |
INTERCEPTED DRUG DISPENSING ERROR | 1 |
Intentional product misuse | 1 |
INTENTIONAL DRUG MISUSE | 1 |
Injury associated with device | 1 |
INJECTION SITE WARMTH | 1 |
Injection site paraesthesia | 1 |
INJECTION SITE NODULE | 1 |
INJECTION SITE MASS | 1 |
Injection site infection | 1 |
Injection site hypoaesthesia | 1 |
Injection site discolouration | 1 |
INJECTION SITE CELLULITIS | 1 |
Injection site bruising | 1 |
Injection site atrophy | 1 |
INJECTION SITE ABSCESS | 1 |
INFUSION SITE URTICARIA | 1 |
Infusion site rash | 1 |
Infusion site pruritus | 1 |
Infusion site erythema | 1 |
INFLAMMATORY MYOFIBROBLASTIC TUMOUR | 1 |
Infection | 1 |
Incorrect product administration duration | 1 |
Incorrect drug administration rate | 1 |
Incorrect dosage administered | 1 |
Incontinence | 1 |
Incision site pain | 1 |
Incision site complication | 1 |
Incision site cellulitis | 1 |
Inappropriate antidiuretic hormone secretion | 1 |
Inappropriate affect | 1 |
Inadequate aseptic technique in use of product | 1 |
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY | 1 |
Hypovolaemia | 1 |
HYPOTONY OF EYE | 1 |
HYPOTONIA | 1 |
Hyposmia | 1 |
HYPOPROTHROMBINAEMIA | 1 |
HYPOCOMPLEMENTAEMIA | 1 |
HYPOAESTHESIA FACIAL | 1 |
Hypoacusis | 1 |
HYPERVENTILATION | 1 |
Hyperuricaemia | 1 |
Hypertensive emergency | 1 |
HYPERNATRAEMIA | 1 |
Hyperchlorhydria | 1 |
Hypercapnia | 1 |
Hot flush | 1 |
Hiccups | 1 |
HIATUS HERNIA | 1 |
Herpes zoster | 1 |
Hepatorenal syndrome | 1 |
HEPATOCELLULAR INJURY | 1 |
Hepatitis acute | 1 |
HEPATITIS | 1 |
HEPATIC HAEMORRHAGE | 1 |
HEPATIC ENZYME ABNORMAL | 1 |
HEPATIC CONGESTION | 1 |
Henoch-Schonlein purpura | 1 |
HEMIPLEGIA | 1 |
Heart sounds abnormal | 1 |
HEARING IMPAIRED | 1 |
HEAD TITUBATION | 1 |
HALLUCINATION, AUDITORY | 1 |
HAEMORRHAGIC EROSIVE GASTRITIS | 1 |
HAEMOLYSIS | 1 |
Haemoglobin abnormal | 1 |
HAEMODIALYSIS | 1 |
Haematoma evacuation | 1 |
Haematocrit abnormal | 1 |
GROIN PAIN | 1 |
Granuloma | 1 |
Gram stain | 1 |
GLOSSITIS | 1 |
GLOMERULONEPHRITIS MINIMAL LESION | 1 |
Glomerular filtration rate decreased | 1 |
Glaucoma | 1 |
GASTROINTESTINAL ULCER HAEMORRHAGE | 1 |
GASTROINTESTINAL NECROSIS | 1 |
Gastrointestinal motility disorder | 1 |
Gastrointestinal ischaemia | 1 |
GASTRIC ULCER PERFORATION | 1 |
Gamma-glutamyltransferase increased | 1 |
Gait disturbance | 1 |
FRACTURE | 1 |
Foetal exposure during pregnancy | 1 |
FLUID OVERLOAD | 1 |
FLAT ANTERIOR CHAMBER OF EYE | 1 |
Fibrosis | 1 |
FIBROMYALGIA | 1 |
Fibrin deposition on lens postoperative | 1 |
Fibrin | 1 |
Facial paralysis | 1 |
FACE INJURY | 1 |
Eyelash changes | 1 |
Eye oedema | 1 |
Eye injury | 1 |
Exposure to SARS-CoV-2 | 1 |
EXPIRED DRUG ADMINISTERED | 1 |
EXERCISE TOLERANCE DECREASED | 1 |
EUPHORIC MOOD | 1 |
ERYTHEMA MULTIFORME | 1 |
ERUCTATION | 1 |
Epilepsy | 1 |
EOSINOPHILIA | 1 |
Eosinophil count increased | 1 |
Enlarged uvula | 1 |
Energy increased | 1 |
ENCEPHALITIS | 1 |
Embolic stroke | 1 |
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION | 1 |
Electrocardiogram QT prolonged | 1 |
ECHOCARDIOGRAM ABNORMAL | 1 |
ECCHYMOSIS | 1 |
Ear congestion | 1 |
Dysuria | 1 |
Dysstasia | 1 |
Dyspnoea exertional | 1 |
DYSPHEMIA | 1 |
Dyspepsia | 1 |
DYSHIDROSIS | 1 |
Dysgeusia | 1 |
Dysentery | 1 |
Duodenal ulcer repair | 1 |
Duodenal obstruction | 1 |
Dry mouth | 1 |
DRUG TOXICITY | 1 |
DRUG INTERACTION POTENTIATION | 1 |
Drug effect decreased | 1 |
Drug dose omission | 1 |
DRUG DISPENSING ERROR | 1 |
Documented hypersensitivity to administered product | 1 |
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG | 1 |
Disorder of globe | 1 |
Disease progression | 1 |
Discontinued product administered | 1 |
Diplegia | 1 |
DIFFUSE LAMELLAR KERATITIS | 1 |
DIFFICULTY IN WALKING | 1 |
DIARRHOEA HAEMORRHAGIC | 1 |
Diaphragmatic spasm | 1 |
Diabetes mellitus | 1 |
Device issue | 1 |
Dermatitis contact | 1 |
DEMENTIA | 1 |
DEAFNESS | 1 |
CYCLITIC MEMBRANE | 1 |
CYANOSIS | 1 |
CROHN'S DISEASE | 1 |
CORONARY ARTERY STENOSIS | 1 |
CORNEAL TRANSPLANT | 1 |
CORNEAL DEGENERATION | 1 |
CONVERSION DISORDER | 1 |
Contrast media reaction | 1 |
Contraindicated product prescribed | 1 |
CONJUNCTIVAL HYPERAEMIA | 1 |
CONJUNCTIVAL HAEMORRHAGE | 1 |
CONGESTIVE CARDIOMYOPATHY | 1 |
Congenital anomaly | 1 |
Concomitant disease progression | 1 |
COMPARTMENT SYNDROME | 1 |
Colitis microscopic | 1 |
CIRCULATORY COLLAPSE | 1 |
Ciliary muscle spasm | 1 |
CHRONIC OBSTRUCTIVE PULMONARY DISEASE | 1 |
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED | 1 |
Chronic gastritis | 1 |
Choroidal effusion | 1 |
Chorioretinopathy | 1 |
Cholestasis | 1 |
CHOKING SENSATION | 1 |
CHOKING | 1 |
CHEST INJURY | 1 |
Chest crushing | 1 |
Chapped lips | 1 |
CEREBRAL ATROPHY | 1 |
Cerebral amyloid angiopathy | 1 |
CATHETER SITE HAEMORRHAGE | 1 |
CATHETER SITE DISCHARGE | 1 |
CATHETER RELATED COMPLICATION | 1 |
Cardiomyopathy | 1 |
Cardiogenic shock | 1 |
Cardiac ventricular thrombosis | 1 |
CARDIAC PROCEDURE COMPLICATION | 1 |
CARDIAC OUTPUT DECREASED | 1 |
Cardiac failure | 1 |
CARBON DIOXIDE DECREASED | 1 |
CANDIDA SEPSIS | 1 |
Caesarean section | 1 |
Burn oral cavity | 1 |
Bronchiolitis | 1 |
Breath sounds absent | 1 |
Breath sounds abnormal | 1 |
Breast tenderness | 1 |
Bradypnoea | 1 |
BONE PAIN | 1 |
Bone infarction | 1 |
BLOOD POTASSIUM INCREASED | 1 |
Blood pH increased | 1 |
BLOOD LACTATE DEHYDROGENASE INCREASED | 1 |
BLOOD GLUCOSE INCREASED | 1 |
BLOOD ERYTHROPOIETIN DECREASED | 1 |
BLOOD CREATINE ABNORMAL | 1 |
Blood cholesterol increased | 1 |
BLOOD BLISTER | 1 |
BLOOD ALKALINE PHOSPHATASE DECREASED | 1 |
BLOOD ALBUMIN DECREASED | 1 |
Blepharochalasis | 1 |
Bleeding time prolonged | 1 |
BLADDER SPASM | 1 |
BLADDER DILATATION | 1 |
BACTERIAL SEPSIS | 1 |
Bacteraemia | 1 |
AZOTAEMIA | 1 |
AURICULAR SWELLING | 1 |
ATRIAL FIBRILLATION | 1 |
ATELECTASIS | 1 |
Aspiration | 1 |
ASPHYXIA | 1 |
Ascites | 1 |
ARTERIAL THROMBOSIS LIMB | 1 |
AREFLEXIA | 1 |
APNOEIC ATTACK | 1 |
Aortic valve replacement | 1 |
Anxiety disorder | 1 |
ANTERIOR CHAMBER FLARE | 1 |
Anterior chamber fibrin | 1 |
Anterior chamber disorder | 1 |
ANGINA UNSTABLE | 1 |
ANEURYSM | 1 |
Anastomotic ulcer | 1 |
ANAPHYLACTOID REACTION | 1 |
Amputation | 1 |
ALTERED STATE OF CONSCIOUSNESS | 1 |
Allodynia | 1 |
Allergic oedema | 1 |
Alcohol use | 1 |
Aggression | 1 |
Administration site irritation | 1 |
ACUTE RESPIRATORY DISTRESS SYNDROME | 1 |
Acute pulmonary oedema | 1 |
Acute prerenal failure | 1 |
ACUTE MYOCARDIAL INFARCTION | 1 |
ACUTE HEPATIC FAILURE | 1 |
ACUTE ABDOMEN | 1 |
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED | 1 |
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL | 1 |
ACNE | 1 |
Abortion spontaneous | 1 |
ABNORMAL DREAMS | 1 |
ABNORMAL BEHAVIOUR | 1 |
ABDOMINAL INJURY | 1 |
ABASIA | 1 |