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FEMUR FRACTURE ( 22 FDA reports)
FALL ( 19 FDA reports)
DYSPNOEA ( 16 FDA reports)
ARTHRALGIA ( 13 FDA reports)
CEREBROVASCULAR ACCIDENT ( 12 FDA reports)
MOUTH ULCERATION ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
OESOPHAGEAL ULCER ( 11 FDA reports)
COUGH ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
OSTEONECROSIS OF JAW ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
DIARRHOEA ( 9 FDA reports)
MALAISE ( 9 FDA reports)
MYALGIA ( 8 FDA reports)
VOMITING ( 8 FDA reports)
BLISTER ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
DUODENAL ULCER PERFORATION ( 7 FDA reports)
GASTRIC ULCER ( 7 FDA reports)
GASTRITIS ( 7 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 7 FDA reports)
OESOPHAGITIS ( 7 FDA reports)
PAIN ( 7 FDA reports)
PERITONITIS ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
HYPERCALCAEMIA ( 6 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
PAIN IN JAW ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
STRESS FRACTURE ( 6 FDA reports)
ALOPECIA ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
NO THERAPEUTIC RESPONSE ( 5 FDA reports)
PURPURA ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
METASTATIC NEOPLASM ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
RHINITIS ALLERGIC ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
ARTERIAL HAEMORRHAGE ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CLEFT LIP AND PALATE ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NASAL POLYPS ( 3 FDA reports)
NIGHT BLINDNESS ( 3 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 3 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OROANTRAL FISTULA ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PELVIC FRACTURE ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
REFLUX OESOPHAGITIS ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RETCHING ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BRACHYCEPHALY ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CAMPTODACTYLY CONGENITAL ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CLINODACTYLY ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DENTAL DISCOMFORT ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DISLOCATION OF VERTEBRA ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEART TRANSPLANT ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INJURY ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
MICROTIA ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
OESOPHAGEAL ATRESIA ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OSTEOMA CUTIS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PATELLA FRACTURE ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RETROGNATHIA ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COLOBOMA ( 1 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CYST ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTELORISM OF ORBIT ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCCUPATIONAL PROBLEM ENVIRONMENTAL ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL IRRITATION ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OLFACTORY NERVE DISORDER ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERIARTICULAR DISORDER ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT LOT NUMBER ISSUE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RETINAL ARTERY SPASM ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TERATOGENICITY ( 1 FDA reports)
TETANY ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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