Please choose an event type to view the corresponding MedsFacts report:

DYSPNOEA ( 344 FDA reports)
NAUSEA ( 285 FDA reports)
PAIN ( 228 FDA reports)
CONSTIPATION ( 200 FDA reports)
DIARRHOEA ( 159 FDA reports)
ABDOMINAL PAIN ( 153 FDA reports)
ANXIETY ( 153 FDA reports)
CHEST PAIN ( 153 FDA reports)
VOMITING ( 142 FDA reports)
CHEST DISCOMFORT ( 137 FDA reports)
HEADACHE ( 125 FDA reports)
BACK PAIN ( 123 FDA reports)
DIZZINESS ( 121 FDA reports)
FALL ( 112 FDA reports)
FATIGUE ( 107 FDA reports)
OEDEMA PERIPHERAL ( 107 FDA reports)
ASTHENIA ( 106 FDA reports)
DRUG INEFFECTIVE ( 100 FDA reports)
WEIGHT DECREASED ( 97 FDA reports)
PYREXIA ( 96 FDA reports)
DEPRESSION ( 89 FDA reports)
ABDOMINAL PAIN UPPER ( 84 FDA reports)
COUGH ( 81 FDA reports)
PAIN IN EXTREMITY ( 79 FDA reports)
SWELLING ( 73 FDA reports)
DEHYDRATION ( 69 FDA reports)
PNEUMONIA ( 69 FDA reports)
HYPERTENSION ( 68 FDA reports)
ANAEMIA ( 67 FDA reports)
ABDOMINAL DISTENSION ( 66 FDA reports)
ARTHRALGIA ( 61 FDA reports)
HYPOAESTHESIA ( 61 FDA reports)
MUSCLE SPASMS ( 61 FDA reports)
HYPOTENSION ( 60 FDA reports)
MUSCULAR WEAKNESS ( 60 FDA reports)
INSOMNIA ( 59 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 58 FDA reports)
INJURY ( 57 FDA reports)
PARAESTHESIA ( 56 FDA reports)
URINARY TRACT INFECTION ( 56 FDA reports)
BONE DISORDER ( 54 FDA reports)
HYPERHIDROSIS ( 54 FDA reports)
CONFUSIONAL STATE ( 53 FDA reports)
MALAISE ( 53 FDA reports)
PRURITUS ( 53 FDA reports)
RENAL FAILURE ( 52 FDA reports)
SYNCOPE ( 51 FDA reports)
DECREASED APPETITE ( 50 FDA reports)
FEELING ABNORMAL ( 50 FDA reports)
ANHEDONIA ( 48 FDA reports)
EMOTIONAL DISTRESS ( 48 FDA reports)
TREMOR ( 48 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 46 FDA reports)
CEREBROVASCULAR ACCIDENT ( 46 FDA reports)
DIVERTICULUM ( 45 FDA reports)
TACHYCARDIA ( 45 FDA reports)
GAIT DISTURBANCE ( 43 FDA reports)
PAIN IN JAW ( 43 FDA reports)
DYSPEPSIA ( 42 FDA reports)
OSTEOMYELITIS ( 42 FDA reports)
VISION BLURRED ( 41 FDA reports)
BRONCHITIS ( 40 FDA reports)
OSTEONECROSIS OF JAW ( 40 FDA reports)
OROPHARYNGEAL PAIN ( 39 FDA reports)
DYSPHAGIA ( 38 FDA reports)
HYPOPHAGIA ( 38 FDA reports)
CHILLS ( 37 FDA reports)
CONVULSION ( 37 FDA reports)
DEEP VEIN THROMBOSIS ( 37 FDA reports)
IRRITABLE BOWEL SYNDROME ( 37 FDA reports)
SOMNOLENCE ( 37 FDA reports)
WEIGHT INCREASED ( 37 FDA reports)
BLOOD PRESSURE INCREASED ( 36 FDA reports)
MEMORY IMPAIRMENT ( 36 FDA reports)
RASH ( 36 FDA reports)
TOOTH INFECTION ( 36 FDA reports)
LOSS OF CONSCIOUSNESS ( 35 FDA reports)
HEART RATE INCREASED ( 34 FDA reports)
OEDEMA ( 34 FDA reports)
INJECTION SITE PAIN ( 33 FDA reports)
BONE PAIN ( 32 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 32 FDA reports)
DRY MOUTH ( 32 FDA reports)
ECZEMA ( 32 FDA reports)
JAW FRACTURE ( 32 FDA reports)
PALPITATIONS ( 32 FDA reports)
SINUSITIS ( 32 FDA reports)
ARTHRITIS ( 31 FDA reports)
BONE LESION ( 31 FDA reports)
CHOLECYSTITIS CHRONIC ( 31 FDA reports)
MULTIPLE MYELOMA ( 31 FDA reports)
MYOCARDIAL INFARCTION ( 31 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 31 FDA reports)
VERTIGO ( 31 FDA reports)
BLOOD GLUCOSE INCREASED ( 30 FDA reports)
INFLUENZA LIKE ILLNESS ( 30 FDA reports)
MYALGIA ( 30 FDA reports)
RENAL FAILURE ACUTE ( 30 FDA reports)
SLEEP APNOEA SYNDROME ( 30 FDA reports)
DEATH ( 29 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 29 FDA reports)
NEPHROLITHIASIS ( 29 FDA reports)
OSTEOPOROSIS ( 29 FDA reports)
BLOOD POTASSIUM DECREASED ( 28 FDA reports)
DEFORMITY ( 28 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 28 FDA reports)
OVERDOSE ( 28 FDA reports)
SEPSIS ( 28 FDA reports)
IMPAIRED HEALING ( 27 FDA reports)
JAW OPERATION ( 27 FDA reports)
MIGRAINE ( 27 FDA reports)
NIGHT SWEATS ( 27 FDA reports)
SPINAL OSTEOARTHRITIS ( 27 FDA reports)
CHOLELITHIASIS ( 26 FDA reports)
DRUG DOSE OMISSION ( 26 FDA reports)
FLATULENCE ( 26 FDA reports)
PARAESTHESIA ORAL ( 26 FDA reports)
PULMONARY EMBOLISM ( 26 FDA reports)
RENAL IMPAIRMENT ( 26 FDA reports)
RESPIRATORY FAILURE ( 26 FDA reports)
TOOTH DISORDER ( 26 FDA reports)
TOOTH FRACTURE ( 26 FDA reports)
CONDITION AGGRAVATED ( 25 FDA reports)
ERYTHEMA ( 25 FDA reports)
FLUSHING ( 25 FDA reports)
METASTASES TO BONE ( 25 FDA reports)
NECK PAIN ( 25 FDA reports)
SKIN DISORDER ( 25 FDA reports)
TOOTH EXTRACTION ( 25 FDA reports)
ASTHMA ( 24 FDA reports)
BACTERAEMIA ( 24 FDA reports)
DYSURIA ( 24 FDA reports)
HYPERKERATOSIS ( 24 FDA reports)
INFECTION ( 24 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 24 FDA reports)
LOOSE TOOTH ( 24 FDA reports)
LYMPHADENOPATHY ( 24 FDA reports)
OSTEONECROSIS ( 24 FDA reports)
SWELLING FACE ( 24 FDA reports)
ABDOMINAL DISCOMFORT ( 23 FDA reports)
ANGIOPATHY ( 23 FDA reports)
BONE EROSION ( 23 FDA reports)
BONE FRAGMENTATION ( 23 FDA reports)
DERMATITIS ( 23 FDA reports)
ECONOMIC PROBLEM ( 23 FDA reports)
ECZEMA ASTEATOTIC ( 23 FDA reports)
ENDODONTIC PROCEDURE ( 23 FDA reports)
FIBROUS HISTIOCYTOMA ( 23 FDA reports)
HYPERLIPIDAEMIA ( 23 FDA reports)
ICHTHYOSIS ( 23 FDA reports)
MITRAL VALVE PROLAPSE ( 23 FDA reports)
ORAL CAVITY FISTULA ( 23 FDA reports)
ORAL MUCOSA ATROPHY ( 23 FDA reports)
PURULENT DISCHARGE ( 23 FDA reports)
TOOTH LOSS ( 23 FDA reports)
UTERINE LEIOMYOMA ( 23 FDA reports)
CONTUSION ( 22 FDA reports)
CYSTITIS ( 22 FDA reports)
NECK INJURY ( 22 FDA reports)
NEUROPATHY PERIPHERAL ( 22 FDA reports)
BONE DENSITY DECREASED ( 21 FDA reports)
DYSPNOEA EXERTIONAL ( 21 FDA reports)
GASTROINTESTINAL DISORDER ( 21 FDA reports)
HALLUCINATION ( 21 FDA reports)
LUNG NEOPLASM ( 21 FDA reports)
ORTHODONTIC APPLIANCE USER ( 21 FDA reports)
RECTAL HAEMORRHAGE ( 21 FDA reports)
RENAL DISORDER ( 21 FDA reports)
ACTINOMYCOSIS ( 20 FDA reports)
DYSKINESIA ( 20 FDA reports)
FLUID OVERLOAD ( 20 FDA reports)
GASTRIC DISORDER ( 20 FDA reports)
HAEMATOCHEZIA ( 20 FDA reports)
HAEMATURIA ( 20 FDA reports)
HYPERSENSITIVITY ( 20 FDA reports)
INFLAMMATION ( 20 FDA reports)
MUCOSAL INFLAMMATION ( 20 FDA reports)
SKIN NEOPLASM EXCISION ( 20 FDA reports)
STEM CELL TRANSPLANT ( 20 FDA reports)
THROAT TIGHTNESS ( 20 FDA reports)
THYROID CANCER ( 20 FDA reports)
TOOTH ABSCESS ( 20 FDA reports)
AMNESIA ( 19 FDA reports)
BLOOD PRESSURE DECREASED ( 19 FDA reports)
CARDIOMYOPATHY ( 19 FDA reports)
CEREBRAL ATROPHY ( 19 FDA reports)
COLITIS ISCHAEMIC ( 19 FDA reports)
DRUG EFFECT DECREASED ( 19 FDA reports)
DRUG HYPERSENSITIVITY ( 19 FDA reports)
FISTULA ( 19 FDA reports)
HALLUCINATION, AUDITORY ( 19 FDA reports)
HYPONATRAEMIA ( 19 FDA reports)
HYPOVOLAEMIA ( 19 FDA reports)
JAW DISORDER ( 19 FDA reports)
NERVOUSNESS ( 19 FDA reports)
RETCHING ( 19 FDA reports)
SUICIDE ATTEMPT ( 19 FDA reports)
THROMBOSIS ( 19 FDA reports)
THYROID NEOPLASM ( 19 FDA reports)
CANDIDIASIS ( 18 FDA reports)
CARDIOMEGALY ( 18 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 18 FDA reports)
HAEMATEMESIS ( 18 FDA reports)
JOINT EFFUSION ( 18 FDA reports)
MALNUTRITION ( 18 FDA reports)
NEURALGIA ( 18 FDA reports)
ORAL PAIN ( 18 FDA reports)
PRIMARY SEQUESTRUM ( 18 FDA reports)
RESORPTION BONE INCREASED ( 18 FDA reports)
THROMBOCYTOPENIA ( 18 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 17 FDA reports)
AZOTAEMIA ( 17 FDA reports)
CELLULITIS ( 17 FDA reports)
DIABETES MELLITUS ( 17 FDA reports)
EYE PAIN ( 17 FDA reports)
GALLBLADDER DISORDER ( 17 FDA reports)
INJECTION SITE ERYTHEMA ( 17 FDA reports)
LUNG DISORDER ( 17 FDA reports)
NEUTROPENIA ( 17 FDA reports)
OSTEOARTHRITIS ( 17 FDA reports)
OSTEOSCLEROSIS ( 17 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 17 FDA reports)
PLEURAL EFFUSION ( 17 FDA reports)
ROAD TRAFFIC ACCIDENT ( 17 FDA reports)
SPINAL COLUMN STENOSIS ( 17 FDA reports)
STRESS ( 17 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 17 FDA reports)
ABDOMINAL HERNIA ( 16 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 16 FDA reports)
BLINDNESS ( 16 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 16 FDA reports)
CHOLECYSTITIS ( 16 FDA reports)
DYSARTHRIA ( 16 FDA reports)
EPISTAXIS ( 16 FDA reports)
FEAR ( 16 FDA reports)
GINGIVAL RECESSION ( 16 FDA reports)
ILEUS ( 16 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 16 FDA reports)
LIGAMENT SPRAIN ( 16 FDA reports)
METASTASES TO ADRENALS ( 16 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 16 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 16 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 16 FDA reports)
ONYCHOMYCOSIS ( 16 FDA reports)
OOPHORECTOMY ( 16 FDA reports)
ORAL FIBROMA ( 16 FDA reports)
PANCYTOPENIA ( 16 FDA reports)
PERIODONTAL DISEASE ( 16 FDA reports)
POSTOPERATIVE ILEUS ( 16 FDA reports)
SINUS TACHYCARDIA ( 16 FDA reports)
SPINAL COMPRESSION FRACTURE ( 16 FDA reports)
BALANCE DISORDER ( 15 FDA reports)
COLITIS ( 15 FDA reports)
COLONIC POLYP ( 15 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 15 FDA reports)
CYST ( 15 FDA reports)
DENTAL FISTULA ( 15 FDA reports)
EJECTION FRACTION DECREASED ( 15 FDA reports)
EMOTIONAL DISORDER ( 15 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 15 FDA reports)
GYNAECOMASTIA ( 15 FDA reports)
HYPOAESTHESIA ORAL ( 15 FDA reports)
LETHARGY ( 15 FDA reports)
MANIA ( 15 FDA reports)
OFF LABEL USE ( 15 FDA reports)
OSTEOPENIA ( 15 FDA reports)
PLASMACYTOSIS ( 15 FDA reports)
POLYURIA ( 15 FDA reports)
TONGUE COATED ( 15 FDA reports)
URINARY INCONTINENCE ( 15 FDA reports)
URTICARIA ( 15 FDA reports)
WHEEZING ( 15 FDA reports)
ATRIAL FIBRILLATION ( 14 FDA reports)
COGNITIVE DISORDER ( 14 FDA reports)
DEPRESSED MOOD ( 14 FDA reports)
DIURETIC THERAPY ( 14 FDA reports)
HAEMOGLOBIN DECREASED ( 14 FDA reports)
HOT FLUSH ( 14 FDA reports)
JOINT SWELLING ( 14 FDA reports)
MEDICATION ERROR ( 14 FDA reports)
MENTAL DISORDER ( 14 FDA reports)
TARDIVE DYSKINESIA ( 14 FDA reports)
UNRESPONSIVE TO STIMULI ( 14 FDA reports)
ALOPECIA ( 13 FDA reports)
ARTERIOSCLEROSIS ( 13 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 13 FDA reports)
BLINDNESS TRANSIENT ( 13 FDA reports)
BURNING SENSATION ( 13 FDA reports)
CARDIAC DISORDER ( 13 FDA reports)
CHRONIC SINUSITIS ( 13 FDA reports)
CORONARY ARTERY DISEASE ( 13 FDA reports)
DENTAL CARIES ( 13 FDA reports)
DIVERTICULITIS ( 13 FDA reports)
GASTRIC ULCER ( 13 FDA reports)
GASTRITIS ( 13 FDA reports)
GINGIVAL GRAFT ( 13 FDA reports)
INJECTION SITE HAEMATOMA ( 13 FDA reports)
METASTASES TO LIVER ( 13 FDA reports)
MICTURITION URGENCY ( 13 FDA reports)
MUSCULOSKELETAL PAIN ( 13 FDA reports)
NASOPHARYNGITIS ( 13 FDA reports)
PRODUCT QUALITY ISSUE ( 13 FDA reports)
PRODUCTIVE COUGH ( 13 FDA reports)
RENAL FAILURE CHRONIC ( 13 FDA reports)
RESTLESSNESS ( 13 FDA reports)
RETINAL HAEMORRHAGE ( 13 FDA reports)
RHINORRHOEA ( 13 FDA reports)
RIB FRACTURE ( 13 FDA reports)
UNEVALUABLE EVENT ( 13 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 13 FDA reports)
URINARY RETENTION ( 13 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 12 FDA reports)
ANOREXIA ( 12 FDA reports)
APHASIA ( 12 FDA reports)
BLISTER ( 12 FDA reports)
BLOOD CREATININE INCREASED ( 12 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 12 FDA reports)
CATARACT ( 12 FDA reports)
CHOLECYSTECTOMY ( 12 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 12 FDA reports)
EARLY SATIETY ( 12 FDA reports)
HAEMORRHOIDS ( 12 FDA reports)
HYPERCHOLESTEROLAEMIA ( 12 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 12 FDA reports)
METASTASES TO LUNG ( 12 FDA reports)
RENAL CYST ( 12 FDA reports)
RESTLESS LEGS SYNDROME ( 12 FDA reports)
STOMATITIS ( 12 FDA reports)
TENDERNESS ( 12 FDA reports)
TOOTHACHE ( 12 FDA reports)
WOUND DEHISCENCE ( 12 FDA reports)
WOUND DRAINAGE ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
BACTERIAL INFECTION ( 11 FDA reports)
BEDRIDDEN ( 11 FDA reports)
BLINDNESS UNILATERAL ( 11 FDA reports)
CHANGE OF BOWEL HABIT ( 11 FDA reports)
COMPRESSION FRACTURE ( 11 FDA reports)
CROHN'S DISEASE ( 11 FDA reports)
EXCORIATION ( 11 FDA reports)
FEMUR FRACTURE ( 11 FDA reports)
HAEMOPTYSIS ( 11 FDA reports)
HYPERTENSIVE CRISIS ( 11 FDA reports)
INJECTION SITE PRURITUS ( 11 FDA reports)
INJECTION SITE REACTION ( 11 FDA reports)
INJECTION SITE SWELLING ( 11 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 11 FDA reports)
INTESTINAL OBSTRUCTION ( 11 FDA reports)
LEUKOPENIA ( 11 FDA reports)
LUMBAR SPINAL STENOSIS ( 11 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 11 FDA reports)
OBESITY ( 11 FDA reports)
OESOPHAGITIS ( 11 FDA reports)
PULMONARY GRANULOMA ( 11 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 11 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 11 FDA reports)
ABNORMAL DREAMS ( 10 FDA reports)
AGITATION ( 10 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 10 FDA reports)
BONE SCAN ABNORMAL ( 10 FDA reports)
DECUBITUS ULCER ( 10 FDA reports)
DIPLOPIA ( 10 FDA reports)
DIZZINESS POSTURAL ( 10 FDA reports)
ELECTROLYTE IMBALANCE ( 10 FDA reports)
ERECTILE DYSFUNCTION ( 10 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 10 FDA reports)
FIBROMYALGIA ( 10 FDA reports)
GINGIVAL DISORDER ( 10 FDA reports)
GOITRE ( 10 FDA reports)
HIP FRACTURE ( 10 FDA reports)
HYPERPARATHYROIDISM ( 10 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 10 FDA reports)
JOINT SPRAIN ( 10 FDA reports)
KYPHOSIS ( 10 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 10 FDA reports)
MELANOCYTIC NAEVUS ( 10 FDA reports)
METASTASES TO LYMPH NODES ( 10 FDA reports)
MITRAL VALVE INCOMPETENCE ( 10 FDA reports)
MOBILITY DECREASED ( 10 FDA reports)
NOCTURIA ( 10 FDA reports)
OBSTRUCTIVE UROPATHY ( 10 FDA reports)
OCCULT BLOOD POSITIVE ( 10 FDA reports)
OPTIC NEURITIS ( 10 FDA reports)
ORAL DISCHARGE ( 10 FDA reports)
OSTEITIS ( 10 FDA reports)
PARATHYROID TUMOUR BENIGN ( 10 FDA reports)
PARKINSON'S DISEASE ( 10 FDA reports)
PNEUMONITIS ( 10 FDA reports)
RETINAL ISCHAEMIA ( 10 FDA reports)
SUICIDAL IDEATION ( 10 FDA reports)
TREATMENT NONCOMPLIANCE ( 10 FDA reports)
ULCER ( 10 FDA reports)
URINE OUTPUT ( 10 FDA reports)
URINE OUTPUT INCREASED ( 10 FDA reports)
VAGINAL DISCHARGE ( 10 FDA reports)
VISUAL IMPAIRMENT ( 10 FDA reports)
VOMITING PROJECTILE ( 10 FDA reports)
ABDOMINAL TENDERNESS ( 9 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 9 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 9 FDA reports)
ATELECTASIS ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 9 FDA reports)
BLOOD POTASSIUM INCREASED ( 9 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 9 FDA reports)
BONE NEOPLASM MALIGNANT ( 9 FDA reports)
CARPAL TUNNEL SYNDROME ( 9 FDA reports)
DISCOMFORT ( 9 FDA reports)
DUODENAL ULCER ( 9 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 9 FDA reports)
ERUCTATION ( 9 FDA reports)
FAMILY STRESS ( 9 FDA reports)
GASTROINTESTINAL PAIN ( 9 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
HEPATIC STEATOSIS ( 9 FDA reports)
HYPERKALAEMIA ( 9 FDA reports)
HYPOALBUMINAEMIA ( 9 FDA reports)
IMPAIRED DRIVING ABILITY ( 9 FDA reports)
INCORRECT DOSE ADMINISTERED ( 9 FDA reports)
LIVER DISORDER ( 9 FDA reports)
METABOLIC ENCEPHALOPATHY ( 9 FDA reports)
METASTATIC PAIN ( 9 FDA reports)
MULTIPLE SCLEROSIS ( 9 FDA reports)
MUSCULOSKELETAL DISORDER ( 9 FDA reports)
NECK MASS ( 9 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 9 FDA reports)
ORAL INFECTION ( 9 FDA reports)
PARATHYROIDECTOMY ( 9 FDA reports)
PLATELET COUNT INCREASED ( 9 FDA reports)
POLLAKIURIA ( 9 FDA reports)
TEMPERATURE INTOLERANCE ( 9 FDA reports)
TINNITUS ( 9 FDA reports)
TRISMUS ( 9 FDA reports)
VAGINAL INFECTION ( 9 FDA reports)
VIITH NERVE PARALYSIS ( 9 FDA reports)
ADRENAL INSUFFICIENCY ( 8 FDA reports)
ADRENAL MASS ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK ( 8 FDA reports)
BILIARY DYSKINESIA ( 8 FDA reports)
BREAST CANCER RECURRENT ( 8 FDA reports)
CAROTID ARTERY STENOSIS ( 8 FDA reports)
CLUMSINESS ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
DRUG DEPENDENCE ( 8 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 8 FDA reports)
DYSPHONIA ( 8 FDA reports)
ESSENTIAL HYPERTENSION ( 8 FDA reports)
EXOSTOSIS ( 8 FDA reports)
FAECAL INCONTINENCE ( 8 FDA reports)
FOOT FRACTURE ( 8 FDA reports)
GASTRODUODENITIS ( 8 FDA reports)
GINGIVAL BLEEDING ( 8 FDA reports)
HEMIPARESIS ( 8 FDA reports)
HIATUS HERNIA ( 8 FDA reports)
HYPERCALCAEMIA ( 8 FDA reports)
HYPOTHYROIDISM ( 8 FDA reports)
INJECTION SITE HAEMORRHAGE ( 8 FDA reports)
LACERATION ( 8 FDA reports)
LIVER SCAN ABNORMAL ( 8 FDA reports)
METASTASES TO THORAX ( 8 FDA reports)
NASAL CONGESTION ( 8 FDA reports)
PANCREATITIS ( 8 FDA reports)
PARALYSIS ( 8 FDA reports)
PHARYNGEAL OEDEMA ( 8 FDA reports)
PREGNANCY ( 8 FDA reports)
PRURITUS GENERALISED ( 8 FDA reports)
PSEUDOMONAS INFECTION ( 8 FDA reports)
RENAL VESSEL DISORDER ( 8 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 8 FDA reports)
RHEUMATOID ARTHRITIS ( 8 FDA reports)
SENSORY DISTURBANCE ( 8 FDA reports)
SPINAL FRACTURE ( 8 FDA reports)
SUBDURAL HAEMATOMA ( 8 FDA reports)
SURGERY ( 8 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 8 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 8 FDA reports)
URINARY HESITATION ( 8 FDA reports)
VAGINAL HAEMORRHAGE ( 8 FDA reports)
ABDOMINAL ADHESIONS ( 7 FDA reports)
ABNORMAL BEHAVIOUR ( 7 FDA reports)
ANIMAL BITE ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
BONE DEBRIDEMENT ( 7 FDA reports)
BRONCHOSPASM ( 7 FDA reports)
BURSITIS ( 7 FDA reports)
CARDIAC MURMUR ( 7 FDA reports)
COLD SWEAT ( 7 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 7 FDA reports)
EAR PAIN ( 7 FDA reports)
FAECALOMA ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
FEELING HOT ( 7 FDA reports)
FLUID RETENTION ( 7 FDA reports)
GINGIVAL INFECTION ( 7 FDA reports)
GRAND MAL CONVULSION ( 7 FDA reports)
HAEMOTHORAX ( 7 FDA reports)
HERPES ZOSTER ( 7 FDA reports)
HYDRONEPHROSIS ( 7 FDA reports)
INTENTIONAL DRUG MISUSE ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 7 FDA reports)
MOVEMENT DISORDER ( 7 FDA reports)
MUSCLE TWITCHING ( 7 FDA reports)
MYOSITIS ( 7 FDA reports)
NASAL SEPTUM DISORDER ( 7 FDA reports)
PARAPLEGIA ( 7 FDA reports)
PATHOLOGICAL FRACTURE ( 7 FDA reports)
PERICARDIAL EFFUSION ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
PNEUMOTHORAX ( 7 FDA reports)
POLYDIPSIA ( 7 FDA reports)
POST THROMBOTIC SYNDROME ( 7 FDA reports)
PROTEINURIA ( 7 FDA reports)
PSYCHOTIC DISORDER ( 7 FDA reports)
PULMONARY HYPERTENSION ( 7 FDA reports)
RENAL CELL CARCINOMA ( 7 FDA reports)
RESPIRATORY DISORDER ( 7 FDA reports)
SEASONAL ALLERGY ( 7 FDA reports)
SKIN DISCOLOURATION ( 7 FDA reports)
SKIN FIBROSIS ( 7 FDA reports)
SLEEP DISORDER ( 7 FDA reports)
SOFT TISSUE INJURY ( 7 FDA reports)
STRESS FRACTURE ( 7 FDA reports)
TRIGEMINAL NEURALGIA ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ACCIDENTAL EXPOSURE ( 6 FDA reports)
ADNEXA UTERI CYST ( 6 FDA reports)
AFFECTIVE DISORDER ( 6 FDA reports)
ANGER ( 6 FDA reports)
ANGIOMYOLIPOMA ( 6 FDA reports)
ATRIAL SEPTAL DEFECT ( 6 FDA reports)
BIPOLAR DISORDER ( 6 FDA reports)
BLOOD GLUCOSE DECREASED ( 6 FDA reports)
BLOOD IRON DECREASED ( 6 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 6 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 6 FDA reports)
CARDIAC VALVE VEGETATION ( 6 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 6 FDA reports)
CLAVICLE FRACTURE ( 6 FDA reports)
DECREASED INTEREST ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DEVICE MALFUNCTION ( 6 FDA reports)
DEVICE RELATED INFECTION ( 6 FDA reports)
DILATATION ATRIAL ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 6 FDA reports)
DRUG ADMINISTRATION ERROR ( 6 FDA reports)
DRUG TOLERANCE ( 6 FDA reports)
DYSSTASIA ( 6 FDA reports)
ENDOCARDITIS ( 6 FDA reports)
EYE SWELLING ( 6 FDA reports)
FACE INJURY ( 6 FDA reports)
FACE OEDEMA ( 6 FDA reports)
GASTROENTERITIS VIRAL ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
GLAUCOMA ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HEART RATE DECREASED ( 6 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 6 FDA reports)
HYPERTHYROIDISM ( 6 FDA reports)
HYPOAESTHESIA FACIAL ( 6 FDA reports)
INTRACRANIAL HYPOTENSION ( 6 FDA reports)
LARYNGITIS ( 6 FDA reports)
LIP SWELLING ( 6 FDA reports)
LIPID METABOLISM DISORDER ( 6 FDA reports)
LUNG NEOPLASM MALIGNANT ( 6 FDA reports)
MEDICATION RESIDUE ( 6 FDA reports)
METABOLIC SYNDROME ( 6 FDA reports)
MULTIPLE INJURIES ( 6 FDA reports)
NERVE COMPRESSION ( 6 FDA reports)
NEUROGENIC BLADDER ( 6 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 6 FDA reports)
ODYNOPHAGIA ( 6 FDA reports)
ORAL HERPES ( 6 FDA reports)
OSTEOCHONDROSIS ( 6 FDA reports)
OSTEOLYSIS ( 6 FDA reports)
OVARIAN CYST ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
PANIC ATTACK ( 6 FDA reports)
PNEUMONIA ASPIRATION ( 6 FDA reports)
PRESYNCOPE ( 6 FDA reports)
PRODUCT ADHESION ISSUE ( 6 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 6 FDA reports)
REGURGITATION ( 6 FDA reports)
RENAL CANCER ( 6 FDA reports)
RENAL MASS ( 6 FDA reports)
SCIATICA ( 6 FDA reports)
SKIN WARM ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
SPLENOMEGALY ( 6 FDA reports)
SYNCOPE VASOVAGAL ( 6 FDA reports)
TEARFULNESS ( 6 FDA reports)
TENSION ( 6 FDA reports)
THYROID CYST ( 6 FDA reports)
TYPE 2 DIABETES MELLITUS ( 6 FDA reports)
UNDERDOSE ( 6 FDA reports)
URINE COLOUR ABNORMAL ( 6 FDA reports)
VASCULAR INSUFFICIENCY ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
WITHDRAWAL SYNDROME ( 6 FDA reports)
ABSCESS ORAL ( 5 FDA reports)
ACTINIC KERATOSIS ( 5 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
AKATHISIA ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
ANKLE FRACTURE ( 5 FDA reports)
BACK INJURY ( 5 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
CATHETERISATION CARDIAC ( 5 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 5 FDA reports)
CONVERSION DISORDER ( 5 FDA reports)
CRYING ( 5 FDA reports)
CUBITAL TUNNEL SYNDROME ( 5 FDA reports)
DYSTONIA ( 5 FDA reports)
ECCHYMOSIS ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
EPICONDYLITIS ( 5 FDA reports)
FACIAL PALSY ( 5 FDA reports)
FIBROSIS ( 5 FDA reports)
FLANK PAIN ( 5 FDA reports)
FRACTURE NONUNION ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 5 FDA reports)
GASTRIC CANCER ( 5 FDA reports)
GASTRITIS EROSIVE ( 5 FDA reports)
GENITAL HERPES ( 5 FDA reports)
GINGIVAL OEDEMA ( 5 FDA reports)
HAEMATOMA ( 5 FDA reports)
HEART RATE IRREGULAR ( 5 FDA reports)
HIP ARTHROPLASTY ( 5 FDA reports)
HOSPITALISATION ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
ILL-DEFINED DISORDER ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
INAPPROPRIATE AFFECT ( 5 FDA reports)
INDURATION ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
JOINT STIFFNESS ( 5 FDA reports)
LABILE HYPERTENSION ( 5 FDA reports)
LOW TURNOVER OSTEOPATHY ( 5 FDA reports)
MACULAR OEDEMA ( 5 FDA reports)
MENOPAUSE ( 5 FDA reports)
METASTASES TO MENINGES ( 5 FDA reports)
MITRAL VALVE REPAIR ( 5 FDA reports)
MOUTH INJURY ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
MUSCLE TIGHTNESS ( 5 FDA reports)
NO THERAPEUTIC RESPONSE ( 5 FDA reports)
PELVIC FRACTURE ( 5 FDA reports)
PELVIC HAEMATOMA ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
POOR DENTAL CONDITION ( 5 FDA reports)
POST PROCEDURAL COMPLICATION ( 5 FDA reports)
POSTMENOPAUSE ( 5 FDA reports)
PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
RENAL INJURY ( 5 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 5 FDA reports)
RHINITIS ALLERGIC ( 5 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 5 FDA reports)
SKIN ATROPHY ( 5 FDA reports)
SKIN TURGOR DECREASED ( 5 FDA reports)
SOCIAL PROBLEM ( 5 FDA reports)
THROAT IRRITATION ( 5 FDA reports)
TORSADE DE POINTES ( 5 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 5 FDA reports)
UPPER LIMB FRACTURE ( 5 FDA reports)
UTERINE DISORDER ( 5 FDA reports)
VARICOSE VEIN ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
VITAMIN B12 DEFICIENCY ( 5 FDA reports)
VULVAL DISORDER ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ADENOIDAL DISORDER ( 4 FDA reports)
AGEUSIA ( 4 FDA reports)
ALVEOLOPLASTY ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ASCITES ( 4 FDA reports)
BACK DISORDER ( 4 FDA reports)
BIPOLAR I DISORDER ( 4 FDA reports)
BLOOD CHLORIDE DECREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BONE CANCER METASTATIC ( 4 FDA reports)
BREAST CANCER METASTATIC ( 4 FDA reports)
CARDIAC ENZYMES INCREASED ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CAROTID ARTERY DISEASE ( 4 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 4 FDA reports)
CEREBELLAR INFARCTION ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CERVICAL SPINAL STENOSIS ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 4 FDA reports)
DETRUSOR SPHINCTER DYSSYNERGIA ( 4 FDA reports)
DEVICE FAILURE ( 4 FDA reports)
DRY EYE ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 4 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
GALLBLADDER INJURY ( 4 FDA reports)
GALLBLADDER PAIN ( 4 FDA reports)
GASTRIC DILATATION ( 4 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 4 FDA reports)
HAIR DISORDER ( 4 FDA reports)
HEPATIC LESION ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 4 FDA reports)
HERNIA ( 4 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
HYSTERECTOMY ( 4 FDA reports)
INCISIONAL DRAINAGE ( 4 FDA reports)
INFLUENZA ( 4 FDA reports)
INITIAL INSOMNIA ( 4 FDA reports)
INTERMITTENT CLAUDICATION ( 4 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 4 FDA reports)
JOINT INJURY ( 4 FDA reports)
LACRIMATION INCREASED ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
METASTASES TO SPINE ( 4 FDA reports)
MIDDLE INSOMNIA ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
NODULE ( 4 FDA reports)
NODULE ON EXTREMITY ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
ORAL SURGERY ( 4 FDA reports)
OSTEOMALACIA ( 4 FDA reports)
PAINFUL RESPIRATION ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PANIC REACTION ( 4 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 4 FDA reports)
PROCEDURAL COMPLICATION ( 4 FDA reports)
PROCTALGIA ( 4 FDA reports)
PROTEIN TOTAL DECREASED ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SCAR ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SINUS DISORDER ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 4 FDA reports)
THERAPY REGIMEN CHANGED ( 4 FDA reports)
THINKING ABNORMAL ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
TONSILLAR DISORDER ( 4 FDA reports)
VOLVULUS ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABSCESS DRAINAGE ( 3 FDA reports)
ACANTHOLYSIS ( 3 FDA reports)
ACUTE PHASE REACTION ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
ALLODYNIA ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANION GAP DECREASED ( 3 FDA reports)
ANORECTAL DISCOMFORT ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
APPLICATION SITE VESICLES ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
BENIGN TUMOUR EXCISION ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD PROLACTIN INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BONE LOSS ( 3 FDA reports)
CARCINOID TUMOUR ( 3 FDA reports)
CARCINOMA IN SITU ( 3 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 3 FDA reports)
CD4/CD8 RATIO DECREASED ( 3 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 3 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHOREA ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DEVICE LEAKAGE ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DISABILITY ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSKINESIA OESOPHAGEAL ( 3 FDA reports)
DYSLIPIDAEMIA ( 3 FDA reports)
EMBOLIC STROKE ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
EYE IRRITATION ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
GASTRIC BYPASS ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GASTROINTESTINAL CARCINOMA ( 3 FDA reports)
GENITAL PAIN ( 3 FDA reports)
GINGIVITIS ( 3 FDA reports)
GOUT ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HIGH FREQUENCY ABLATION ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
INADEQUATE ANALGESIA ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 3 FDA reports)
INJECTION SITE CYST ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INJECTION SITE MASS ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
MENSTRUAL DISORDER ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 3 FDA reports)
MONOCYTE COUNT INCREASED ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MUSCLE INJURY ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NASAL DISORDER ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
NITRITE URINE PRESENT ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
OBSTRUCTION GASTRIC ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PACHYMENINGITIS ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PARACENTESIS ( 3 FDA reports)
PENILE PROSTHESIS INSERTION ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
POLYCYSTIC OVARIES ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
POSTNASAL DRIP ( 3 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 3 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PUPIL FIXED ( 3 FDA reports)
RADIOTHERAPY ( 3 FDA reports)
RALES ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
SCOLIOSIS ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 3 FDA reports)
SPINAL CORD DISORDER ( 3 FDA reports)
SPINAL DEFORMITY ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
THYROIDECTOMY ( 3 FDA reports)
TOOTH REPAIR ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VEIN PAIN ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
WALKING AID USER ( 3 FDA reports)
YELLOW SKIN ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADHESIOLYSIS ( 2 FDA reports)
ADRENAL HAEMORRHAGE ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC VALVE CALCIFICATION ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APNOEA ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BREAST ENLARGEMENT ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHOLESTEROSIS ( 2 FDA reports)
CLUSTER HEADACHE ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERYTHEMA ANNULARE ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GRIMACING ( 2 FDA reports)
GUN SHOT WOUND ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 2 FDA reports)
HEPATIC ADENOMA ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOPNOEA ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE INSERTION ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
LIVER OPERATION ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METASTASES TO KIDNEY ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUCOSAL EXCORIATION ( 2 FDA reports)
NASAL SEPTAL OPERATION ( 2 FDA reports)
NEOPLASM SKIN ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERIVASCULAR DERMATITIS ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 2 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 2 FDA reports)
PROSTATE CANCER RECURRENT ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN DISCOMFORT ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
STARING ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
TERMINAL INSOMNIA ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
ULNAR NERVE INJURY ( 2 FDA reports)
URETHRAL CARUNCLE ( 2 FDA reports)
URETHRAL POLYP ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
VAGINAL PROLAPSE ( 2 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VERTEBROPLASTY ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
WOUND ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE NODULE ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BASILAR MIGRAINE ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHEST WALL MASS ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CRYSTAL DEPOSIT INTESTINE ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EPIDURAL ANAESTHESIA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HOLMES-ADIE PUPIL ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPHAEMA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JC VIRUS TEST POSITIVE ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
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LIMB DISCOMFORT ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
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LOCAL SWELLING ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
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LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
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LUNG OPERATION ( 1 FDA reports)
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LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MACULAR RUPTURE ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 1 FDA reports)
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MASS ( 1 FDA reports)
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MASTOIDITIS ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
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MENSTRUATION IRREGULAR ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NASOGASTRIC OUTPUT HIGH ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
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NEUROLOGICAL SYMPTOM ( 1 FDA reports)
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NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
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OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSCILLOPSIA ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVULATION PAIN ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
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PARAPARESIS ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
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PHARYNGITIS ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
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PITYRIASIS ROSEA ( 1 FDA reports)
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POLYP ( 1 FDA reports)
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PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PRESBYOESOPHAGUS ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
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RASH FOLLICULAR ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCLERAL CYST ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
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SENSORY LOSS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
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SLUGGISHNESS ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
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SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
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SPUTUM PURULENT ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
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STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
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UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
URETERIC CANCER ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
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URTICARIA GENERALISED ( 1 FDA reports)
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UTERINE POLYP ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
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WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
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WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
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