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

COMPLETED SUICIDE ( 223 FDA reports)
CARDIAC ARREST ( 115 FDA reports)
RESPIRATORY ARREST ( 114 FDA reports)
PAIN ( 70 FDA reports)
DEATH ( 68 FDA reports)
NAUSEA ( 65 FDA reports)
CARDIO-RESPIRATORY ARREST ( 59 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 53 FDA reports)
HEADACHE ( 49 FDA reports)
VOMITING ( 49 FDA reports)
MULTIPLE DRUG OVERDOSE ( 47 FDA reports)
POISONING ( 44 FDA reports)
PAIN IN EXTREMITY ( 43 FDA reports)
DRUG TOXICITY ( 42 FDA reports)
INTENTIONAL DRUG MISUSE ( 42 FDA reports)
ANXIETY ( 40 FDA reports)
SOMNOLENCE ( 40 FDA reports)
DYSPNOEA ( 39 FDA reports)
DRUG INEFFECTIVE ( 38 FDA reports)
CONFUSIONAL STATE ( 36 FDA reports)
PARAESTHESIA ( 33 FDA reports)
DEEP VEIN THROMBOSIS ( 31 FDA reports)
FATIGUE ( 31 FDA reports)
ASTHENIA ( 30 FDA reports)
DRUG ABUSE ( 30 FDA reports)
PULMONARY EMBOLISM ( 29 FDA reports)
DIARRHOEA ( 28 FDA reports)
FALL ( 28 FDA reports)
LETHARGY ( 28 FDA reports)
OVERDOSE ( 28 FDA reports)
BACK PAIN ( 27 FDA reports)
MYOCARDIAL INFARCTION ( 27 FDA reports)
PYREXIA ( 27 FDA reports)
ARTHRALGIA ( 26 FDA reports)
DEHYDRATION ( 26 FDA reports)
LOSS OF CONSCIOUSNESS ( 26 FDA reports)
PNEUMONIA ( 26 FDA reports)
COMA ( 25 FDA reports)
DIZZINESS ( 25 FDA reports)
HYPOTENSION ( 25 FDA reports)
HYPERTENSION ( 24 FDA reports)
OEDEMA PERIPHERAL ( 24 FDA reports)
AGITATION ( 23 FDA reports)
HAEMOGLOBIN DECREASED ( 23 FDA reports)
HYPERHIDROSIS ( 23 FDA reports)
ROAD TRAFFIC ACCIDENT ( 23 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 22 FDA reports)
DEPRESSION ( 22 FDA reports)
SINUS TACHYCARDIA ( 22 FDA reports)
ANAEMIA ( 21 FDA reports)
DRUG ABUSER ( 21 FDA reports)
HYPOAESTHESIA ( 21 FDA reports)
INSOMNIA ( 21 FDA reports)
MALAISE ( 21 FDA reports)
RENAL FAILURE ACUTE ( 21 FDA reports)
CHILLS ( 20 FDA reports)
PLEURAL EFFUSION ( 20 FDA reports)
CHEST PAIN ( 19 FDA reports)
ERYTHEMA ( 19 FDA reports)
RASH ( 19 FDA reports)
TACHYCARDIA ( 19 FDA reports)
ABDOMINAL PAIN ( 18 FDA reports)
CELLULITIS ( 18 FDA reports)
DRUG DEPENDENCE ( 18 FDA reports)
URINARY TRACT INFECTION ( 18 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
CHOLECYSTITIS CHRONIC ( 17 FDA reports)
COUGH ( 17 FDA reports)
INJURY ( 17 FDA reports)
OXYGEN SATURATION DECREASED ( 17 FDA reports)
BLOOD CREATININE INCREASED ( 16 FDA reports)
DECREASED APPETITE ( 16 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
BLOOD UREA INCREASED ( 15 FDA reports)
CHOLELITHIASIS ( 15 FDA reports)
BLOOD POTASSIUM DECREASED ( 14 FDA reports)
MENTAL STATUS CHANGES ( 14 FDA reports)
WEIGHT DECREASED ( 14 FDA reports)
BLOOD GLUCOSE INCREASED ( 13 FDA reports)
CARDIOMYOPATHY ( 13 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 13 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 13 FDA reports)
HAEMATOCRIT DECREASED ( 13 FDA reports)
HYPOKALAEMIA ( 13 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 13 FDA reports)
POLYSUBSTANCE ABUSE ( 13 FDA reports)
RASH ERYTHEMATOUS ( 13 FDA reports)
RHEUMATOID ARTHRITIS ( 13 FDA reports)
SUICIDE ATTEMPT ( 13 FDA reports)
AMNESIA ( 12 FDA reports)
BRONCHITIS ( 12 FDA reports)
CONVULSION ( 12 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 12 FDA reports)
EMOTIONAL DISTRESS ( 12 FDA reports)
EPISTAXIS ( 12 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 12 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 12 FDA reports)
IMMUNOSUPPRESSION ( 12 FDA reports)
INTENTIONAL MISUSE ( 12 FDA reports)
MUSCULAR WEAKNESS ( 12 FDA reports)
MUSCULOSKELETAL PAIN ( 12 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 12 FDA reports)
PALPITATIONS ( 12 FDA reports)
PRURITUS ( 12 FDA reports)
TREMOR ( 12 FDA reports)
CATARACT ( 11 FDA reports)
HEART RATE INCREASED ( 11 FDA reports)
ILEUS PARALYTIC ( 11 FDA reports)
MENTAL DISORDER ( 11 FDA reports)
MUSCLE SPASMS ( 11 FDA reports)
SEPSIS ( 11 FDA reports)
ANGIOEDEMA ( 10 FDA reports)
BLOOD PRESSURE DECREASED ( 10 FDA reports)
CYANOSIS ( 10 FDA reports)
GALLBLADDER DISORDER ( 10 FDA reports)
GROIN PAIN ( 10 FDA reports)
INCORRECT DOSE ADMINISTERED ( 10 FDA reports)
MEDICATION ERROR ( 10 FDA reports)
NECK PAIN ( 10 FDA reports)
SINUSITIS ( 10 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 10 FDA reports)
VASODILATATION ( 10 FDA reports)
VISUAL IMPAIRMENT ( 10 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 10 FDA reports)
ACCIDENTAL OVERDOSE ( 9 FDA reports)
BLOOD ALBUMIN DECREASED ( 9 FDA reports)
DELIRIUM ( 9 FDA reports)
DISORIENTATION ( 9 FDA reports)
DRUG HYPERSENSITIVITY ( 9 FDA reports)
HAEMATURIA ( 9 FDA reports)
HYPERLIPIDAEMIA ( 9 FDA reports)
INTENTIONAL OVERDOSE ( 9 FDA reports)
NEUROPATHY PERIPHERAL ( 9 FDA reports)
PANCREATITIS ( 9 FDA reports)
PANCREATITIS ACUTE ( 9 FDA reports)
POST PROCEDURAL COMPLICATION ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
RASH PRURITIC ( 9 FDA reports)
SWELLING FACE ( 9 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 9 FDA reports)
ANGER ( 8 FDA reports)
BLISTER ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 8 FDA reports)
BLOOD SODIUM DECREASED ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 8 FDA reports)
CHOLECYSTECTOMY ( 8 FDA reports)
CONTUSION ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
HYPERSENSITIVITY ( 8 FDA reports)
HYPERSOMNIA ( 8 FDA reports)
MACULAR OEDEMA ( 8 FDA reports)
MYALGIA ( 8 FDA reports)
NEURALGIA ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
POSTOPERATIVE ILEUS ( 8 FDA reports)
PROCEDURAL PAIN ( 8 FDA reports)
RASH GENERALISED ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
RENAL FAILURE CHRONIC ( 8 FDA reports)
RESPIRATORY DEPRESSION ( 8 FDA reports)
RESPIRATORY RATE DECREASED ( 8 FDA reports)
RHINORRHOEA ( 8 FDA reports)
URINE OUTPUT DECREASED ( 8 FDA reports)
ACIDOSIS ( 7 FDA reports)
AGGRESSION ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
BODY TEMPERATURE INCREASED ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
CONSTIPATION ( 7 FDA reports)
DISCOMFORT ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
DRUG SCREEN POSITIVE ( 7 FDA reports)
DYSARTHRIA ( 7 FDA reports)
DYSPEPSIA ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
EYE HAEMORRHAGE ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
HEPATIC STEATOSIS ( 7 FDA reports)
HERPES ZOSTER ( 7 FDA reports)
INTESTINAL ISCHAEMIA ( 7 FDA reports)
PERIPHERAL COLDNESS ( 7 FDA reports)
PROTHROMBIN TIME PROLONGED ( 7 FDA reports)
RESPIRATORY RATE INCREASED ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
SOMNAMBULISM ( 7 FDA reports)
SPEECH DISORDER ( 7 FDA reports)
SUICIDAL IDEATION ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
UNRESPONSIVE TO STIMULI ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
ANOREXIA ( 6 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 6 FDA reports)
BLOOD PH DECREASED ( 6 FDA reports)
BLOOD POTASSIUM INCREASED ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 6 FDA reports)
BURNING SENSATION ( 6 FDA reports)
DEPRESSED MOOD ( 6 FDA reports)
DISSOCIATIVE FUGUE ( 6 FDA reports)
HERPES ZOSTER DISSEMINATED ( 6 FDA reports)
IMPAIRED DRIVING ABILITY ( 6 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 6 FDA reports)
INJECTION SITE PAIN ( 6 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 6 FDA reports)
MIOSIS ( 6 FDA reports)
NEPHROLITHIASIS ( 6 FDA reports)
NIGHT SWEATS ( 6 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
OVARIAN CYST ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
PLEOCYTOSIS ( 6 FDA reports)
POST HERPETIC NEURALGIA ( 6 FDA reports)
RASH PAPULOSQUAMOUS ( 6 FDA reports)
RASH PUSTULAR ( 6 FDA reports)
RESTLESSNESS ( 6 FDA reports)
SEROCONVERSION TEST POSITIVE ( 6 FDA reports)
SKIN LESION ( 6 FDA reports)
SKIN OEDEMA ( 6 FDA reports)
SLEEP-RELATED EATING DISORDER ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
TOXOPLASMOSIS ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ANION GAP INCREASED ( 5 FDA reports)
APHAGIA ( 5 FDA reports)
APPENDICECTOMY ( 5 FDA reports)
ARTERIOSCLEROSIS ( 5 FDA reports)
ARTHRITIS ( 5 FDA reports)
BILIARY DYSKINESIA ( 5 FDA reports)
BLOOD CALCIUM DECREASED ( 5 FDA reports)
BLOOD CHLORIDE DECREASED ( 5 FDA reports)
BODY TEMPERATURE DECREASED ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
COGNITIVE DISORDER ( 5 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 5 FDA reports)
DIABETIC RETINOPATHY ( 5 FDA reports)
DRY SKIN ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
FOOT FRACTURE ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 5 FDA reports)
INADEQUATE ANALGESIA ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 5 FDA reports)
LEUKOCYTOSIS ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
MIGRAINE ( 5 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
PERIORBITAL OEDEMA ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 5 FDA reports)
PSORIASIS ( 5 FDA reports)
RASH MACULAR ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
RENAL ARTERY STENOSIS ( 5 FDA reports)
RENAL ATROPHY ( 5 FDA reports)
RENAL TUBULAR NECROSIS ( 5 FDA reports)
SEBORRHOEA ( 5 FDA reports)
SPINAL COLUMN STENOSIS ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
VITH NERVE PARALYSIS ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ACARODERMATITIS ( 4 FDA reports)
ACCIDENTAL DEATH ( 4 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 4 FDA reports)
APPENDICITIS PERFORATED ( 4 FDA reports)
ATAXIA ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
BILIARY COLIC ( 4 FDA reports)
BLEPHARITIS ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BLOOD PRESSURE ABNORMAL ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
COCCIDIOIDOMYCOSIS ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
FACIAL BONES FRACTURE ( 4 FDA reports)
FACTOR VIII INHIBITION ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
GOUT ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
GYNAECOMASTIA ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
ILEUS ( 4 FDA reports)
ILIAC ARTERY THROMBOSIS ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INTESTINAL DILATATION ( 4 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
LACERATION ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
MANIA ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
NEOPLASM PROGRESSION ( 4 FDA reports)
OCCULT BLOOD POSITIVE ( 4 FDA reports)
PERIORBITAL HAEMATOMA ( 4 FDA reports)
PETECHIAE ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PO2 DECREASED ( 4 FDA reports)
POLYCYTHAEMIA ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
PURPURA ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
RESTLESS LEGS SYNDROME ( 4 FDA reports)
SEDATION ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
STRESS ( 4 FDA reports)
TOOTH DISORDER ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
AORTIC ANEURYSM ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CEREBRAL THROMBOSIS ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DEVICE LEAKAGE ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRUG TOLERANCE INCREASED ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 3 FDA reports)
EXCORIATION ( 3 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
GALLBLADDER INJURY ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEPATIC CYST ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HICCUPS ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
KIDNEY SMALL ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NEPHRITIS ALLERGIC ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PAROTITIS ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PO2 ABNORMAL ( 3 FDA reports)
POISONING DELIBERATE ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
POOR VENOUS ACCESS ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
PUPIL FIXED ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RETROPERITONEAL HAEMATOMA ( 3 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SKIN LACERATION ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
SPLENIC GRANULOMA ( 3 FDA reports)
SWELLING ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
URINARY SEDIMENT ABNORMAL ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALCOHOL ABUSE ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BILIARY FIBROSIS ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARCINOMA ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
CORONARY ARTERY SURGERY ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CRYING ( 2 FDA reports)
CSF TEST ABNORMAL ( 2 FDA reports)
CYTOTOXIC OEDEMA ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEFORMITY ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DETOXIFICATION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG SCREEN NEGATIVE ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FINE MOTOR DELAY ( 2 FDA reports)
FOETAL DEATH ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GESTATIONAL TROPHOBLASTIC TUMOUR ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATIC PAIN ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LOSS OF PROPRIOCEPTION ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NEUROGENIC BOWEL ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 2 FDA reports)
PERSEVERATION ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PILOERECTION ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POST PROCEDURAL NAUSEA ( 2 FDA reports)
POST PROCEDURAL VOMITING ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROCEDURAL NAUSEA ( 2 FDA reports)
PROCEDURAL VOMITING ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
RALES ( 2 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCAB ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SKIN FIBROSIS ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
SPINAL CORD INJURY CERVICAL ( 2 FDA reports)
SPONDYLITIC MYELOPATHY ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STOOL ANALYSIS ABNORMAL ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
UMBILICAL HERNIA PERFORATION ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WOUND ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL INJURY ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANGIOSARCOMA ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPLICATION SITE DRYNESS ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOSCLEROTIC GANGRENE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BENIGN LARYNGEAL NEOPLASM ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALCOHOL ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD KETONE BODY INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYST ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMOGRAPHISM ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC END STAGE RENAL DISEASE ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL HEART RATE INCREASED ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
GASTRIC BANDING ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIPLEGIA TRANSIENT ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOOSE BODY IN JOINT ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYOSCLEROSIS ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL POLYPECTOMY ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NELSON'S SYNDROME ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL CAVITY FISTULA ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OSTEOTOMY ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PERIODONTAL INFECTION ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SI QIII TIII PATTERN ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THIRST ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TURNER'S SYNDROME ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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