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

RENAL FAILURE ACUTE ( 24 FDA reports)
URINARY RETENTION ( 23 FDA reports)
DRUG INTERACTION ( 17 FDA reports)
DRUG INEFFECTIVE ( 15 FDA reports)
PYREXIA ( 15 FDA reports)
CHOLESTASIS ( 14 FDA reports)
DIZZINESS ( 14 FDA reports)
CYTOLYTIC HEPATITIS ( 13 FDA reports)
HAEMATURIA ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
PAIN IN EXTREMITY ( 12 FDA reports)
RHABDOMYOLYSIS ( 12 FDA reports)
URINARY TRACT INFECTION ( 12 FDA reports)
DYSPNOEA ( 11 FDA reports)
FALL ( 11 FDA reports)
RENAL FAILURE ( 11 FDA reports)
ABDOMINAL PAIN ( 10 FDA reports)
ANXIETY ( 10 FDA reports)
ASTHENIA ( 10 FDA reports)
ATRIAL FIBRILLATION ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
SEPTIC SHOCK ( 10 FDA reports)
TREMOR ( 10 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
FEELING ABNORMAL ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
PRURITUS ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
ANAEMIA ( 8 FDA reports)
ARTHROPATHY ( 8 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
COORDINATION ABNORMAL ( 8 FDA reports)
HYPERTHERMIA ( 8 FDA reports)
MYALGIA ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
BACK PAIN ( 7 FDA reports)
HALLUCINATION ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
MUSCLE DISORDER ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
SEXUAL DYSFUNCTION ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DEATH ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DRUG EFFECT DECREASED ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
HYPOREFLEXIA ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
MIDDLE INSOMNIA ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
MYOPATHY ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
NOCTURIA ( 6 FDA reports)
OESOPHAGITIS ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
RHEUMATOID ARTHRITIS ( 6 FDA reports)
ROAD TRAFFIC ACCIDENT ( 6 FDA reports)
TENDON RUPTURE ( 6 FDA reports)
WHIPLASH INJURY ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 5 FDA reports)
COLITIS ISCHAEMIC ( 5 FDA reports)
DELIRIUM ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
FINGER DEFORMITY ( 5 FDA reports)
FLUSHING ( 5 FDA reports)
GYNAECOMASTIA ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PROSTATISM ( 5 FDA reports)
RASH ( 5 FDA reports)
SHOULDER PAIN ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
AGITATION ( 4 FDA reports)
APPLICATION SITE ERYTHEMA ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
BREAST PAIN ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HYPERCALCAEMIA ( 4 FDA reports)
HYPOVOLAEMIA ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MUSCLE HAEMORRHAGE ( 4 FDA reports)
MUSCLE STRAIN ( 4 FDA reports)
MYOCLONUS ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PNEUMONIA LEGIONELLA ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASEPTIC NECROSIS BONE ( 3 FDA reports)
BACTERIAL TEST POSITIVE ( 3 FDA reports)
BLADDER DISORDER ( 3 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE III ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BURNS THIRD DEGREE ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
COMA ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PAIN ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
RADICULOPATHY ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC INTRAMURAL HAEMATOMA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APPLICATION SITE BURN ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
APPLICATION SITE VESICLES ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLADDER MASS ( 2 FDA reports)
BLADDER SPASM ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
COLITIS ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INGUINAL HERNIA REPAIR ( 2 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PERIANAL ABSCESS ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMOCOCCAL INFECTION ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROSTATOMEGALY ( 2 FDA reports)
PSEUDOLYMPHOMA ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
TOOTH INJURY ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CD4/CD8 RATIO DECREASED ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OESOPHAGEAL MOTILITY TEST ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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