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

DRUG INEFFECTIVE ( 28 FDA reports)
MYOCARDIAL INFARCTION ( 24 FDA reports)
DIARRHOEA ( 21 FDA reports)
PNEUMONIA ( 21 FDA reports)
RHABDOMYOLYSIS ( 20 FDA reports)
CHEST PAIN ( 17 FDA reports)
FALL ( 16 FDA reports)
INJURY ( 15 FDA reports)
DEATH ( 14 FDA reports)
DEPRESSION ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 14 FDA reports)
NAUSEA ( 14 FDA reports)
EMOTIONAL DISTRESS ( 13 FDA reports)
PAIN IN EXTREMITY ( 13 FDA reports)
CARDIAC DISORDER ( 12 FDA reports)
DEHYDRATION ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 12 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
ANXIETY ( 11 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 11 FDA reports)
CEREBROVASCULAR ACCIDENT ( 11 FDA reports)
DIZZINESS ( 11 FDA reports)
HYPERTENSION ( 11 FDA reports)
MIGRAINE ( 11 FDA reports)
SINUSITIS ( 11 FDA reports)
ADVERSE EVENT ( 10 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 10 FDA reports)
BRONCHITIS ( 10 FDA reports)
HYPERHIDROSIS ( 10 FDA reports)
OSTEOARTHRITIS ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
SEPTIC SHOCK ( 10 FDA reports)
BACK PAIN ( 9 FDA reports)
CORONARY ARTERY DISEASE ( 9 FDA reports)
HAEMATURIA ( 9 FDA reports)
HAEMORRHOIDS ( 9 FDA reports)
HEADACHE ( 9 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 9 FDA reports)
OEDEMA PERIPHERAL ( 9 FDA reports)
SKIN DISCOLOURATION ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
CARDIAC MURMUR ( 8 FDA reports)
CARDIAC VALVE DISEASE ( 8 FDA reports)
CHEST WALL PAIN ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
RECTAL HAEMORRHAGE ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
THROMBOSIS ( 8 FDA reports)
VIRAL INFECTION ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
ARTHRALGIA ( 7 FDA reports)
ASTHMA ( 7 FDA reports)
CELLULITIS ( 7 FDA reports)
CHRONIC FATIGUE SYNDROME ( 7 FDA reports)
CONTUSION ( 7 FDA reports)
DEVICE RELATED INFECTION ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
IRON DEFICIENCY ANAEMIA ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
NASOPHARYNGITIS ( 7 FDA reports)
NECK PAIN ( 7 FDA reports)
SYSTEMIC CANDIDA ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ABDOMINAL PAIN LOWER ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ACUTE HEPATIC FAILURE ( 6 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
ARTHROPATHY ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
GASTROENTERITIS ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
NON-CARDIAC CHEST PAIN ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
VOMITING ( 6 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DRUG ADMINISTRATION ERROR ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
FORMICATION ( 5 FDA reports)
GASTRIC DISORDER ( 5 FDA reports)
GASTRIC HAEMORRHAGE ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
HEART RATE IRREGULAR ( 5 FDA reports)
HYPERCHOLESTEROLAEMIA ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
NEPHROLITHIASIS ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PYELONEPHRITIS ( 5 FDA reports)
SPINAL OSTEOARTHRITIS ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
ACUTE SINUSITIS ( 4 FDA reports)
ANASTOMOTIC ULCER ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
ANGIOPATHY ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
BREAST PAIN ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
FEMUR FRACTURE ( 4 FDA reports)
FIBROADENOMA OF BREAST ( 4 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 4 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMOCHROMATOSIS ( 4 FDA reports)
HAEMORRHAGIC DISORDER ( 4 FDA reports)
HIP ARTHROPLASTY ( 4 FDA reports)
HIRSUTISM ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
LACTOSE INTOLERANCE ( 4 FDA reports)
LICHEN SCLEROSUS ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PREMATURE BABY ( 4 FDA reports)
PROSTATIC DISORDER ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
RESTLESS LEGS SYNDROME ( 4 FDA reports)
SECONDARY HYPOTHYROIDISM ( 4 FDA reports)
SHIGELLA INFECTION ( 4 FDA reports)
SKIN STRIAE ( 4 FDA reports)
SMALL FOR DATES BABY ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
THYROID NEOPLASM ( 4 FDA reports)
TREATMENT FAILURE ( 4 FDA reports)
TREMOR ( 4 FDA reports)
UNDERDOSE ( 4 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 4 FDA reports)
WEIGHT LOSS POOR ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ABSCESS ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
ATHEROSCLEROSIS ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BACK DISORDER ( 3 FDA reports)
BACK INJURY ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BODY HEIGHT DECREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BONE SCAN ABNORMAL ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
COMA ( 3 FDA reports)
CONCUSSION ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FAILURE TO THRIVE ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GINGIVAL PAIN ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
GLIOMA ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTRA-UTERINE DEATH ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PEMPHIGUS ( 3 FDA reports)
PERIODONTAL DISEASE ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PROSTATITIS ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
RIB FRACTURE ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SCHISTOSOMIASIS ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
ULCER ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ASCITES ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
COUGH ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC INFECTION FUNGAL ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
ILEAL PERFORATION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTESTINAL FISTULA ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
MUCOSAL ULCERATION ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PAIN ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETROPERITONEAL ABSCESS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL TRICUSPID VALVE STENOSIS ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 1 FDA reports)
EPIDIDYMAL DISORDER ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NODULE ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SCAR ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRICHOSPORON INFECTION ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)

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