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

PYREXIA ( 46 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 44 FDA reports)
NAUSEA ( 33 FDA reports)
HEADACHE ( 30 FDA reports)
VOMITING ( 28 FDA reports)
DIARRHOEA ( 27 FDA reports)
FATIGUE ( 23 FDA reports)
ANAEMIA ( 21 FDA reports)
RENAL FAILURE ( 21 FDA reports)
RENAL IMPAIRMENT ( 19 FDA reports)
MYALGIA ( 17 FDA reports)
ASTHENIA ( 16 FDA reports)
GLAUCOMA ( 16 FDA reports)
LYMPHADENOPATHY ( 16 FDA reports)
WEIGHT DECREASED ( 16 FDA reports)
VIRAL LOAD INCREASED ( 15 FDA reports)
ABDOMINAL PAIN ( 14 FDA reports)
CEREBROVASCULAR ACCIDENT ( 14 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 14 FDA reports)
HYPONATRAEMIA ( 13 FDA reports)
MYOCARDIAL INFARCTION ( 13 FDA reports)
PAIN ( 13 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
BLOOD BILIRUBIN INCREASED ( 12 FDA reports)
DECREASED APPETITE ( 12 FDA reports)
DIABETES MELLITUS ( 12 FDA reports)
JAUNDICE ( 12 FDA reports)
PAIN IN EXTREMITY ( 12 FDA reports)
UVEITIS ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 11 FDA reports)
CHOLESTASIS OF PREGNANCY ( 11 FDA reports)
DRUG HYPERSENSITIVITY ( 11 FDA reports)
DRUG INTERACTION ( 11 FDA reports)
HYPOKALAEMIA ( 11 FDA reports)
LACTIC ACIDOSIS ( 11 FDA reports)
THROMBOCYTOPENIA ( 11 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
HYPERLIPIDAEMIA ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
PANCREATITIS ACUTE ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
RASH ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
CHILLS ( 9 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
PANCYTOPENIA ( 9 FDA reports)
PNEUMOTHORAX ( 9 FDA reports)
POLYARTHRITIS ( 9 FDA reports)
PREGNANCY ( 9 FDA reports)
ABORTION SPONTANEOUS ( 8 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 8 FDA reports)
ANOGENITAL WARTS ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
LIVER DISORDER ( 8 FDA reports)
METASTASES TO LUNG ( 8 FDA reports)
NEPHROLITHIASIS ( 8 FDA reports)
PHLEBITIS ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
SKIN DEPIGMENTATION ( 8 FDA reports)
SQUAMOUS CELL CARCINOMA ( 8 FDA reports)
ABNORMAL BEHAVIOUR ( 7 FDA reports)
ABORTION INDUCED ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 7 FDA reports)
CARDIAC MALPOSITION ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
DEATH ( 7 FDA reports)
DYSLIPIDAEMIA ( 7 FDA reports)
HEPATIC DISPLACEMENT ( 7 FDA reports)
HYPERBILIRUBINAEMIA ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
ILL-DEFINED DISORDER ( 7 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 7 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 7 FDA reports)
MALAISE ( 7 FDA reports)
PARAESTHESIA ( 7 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 7 FDA reports)
ACNE ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 6 FDA reports)
BLOOD POTASSIUM INCREASED ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
DEPRESSED MOOD ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 6 FDA reports)
ENCEPHALITIS ( 6 FDA reports)
FALL ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
HEMIPARESIS ( 6 FDA reports)
HEPATOCELLULAR INJURY ( 6 FDA reports)
HYPERCHOLESTEROLAEMIA ( 6 FDA reports)
INJECTION SITE ERYTHEMA ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
PHARYNGEAL ULCERATION ( 6 FDA reports)
POOR QUALITY SLEEP ( 6 FDA reports)
PREMATURE BABY ( 6 FDA reports)
RENAL CANCER METASTATIC ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
AIDS ENCEPHALOPATHY ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
APPARENT DEATH ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BLOOD URIC ACID INCREASED ( 5 FDA reports)
CLEFT LIP ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
CYTOLYTIC HEPATITIS ( 5 FDA reports)
EOSINOPHILIA ( 5 FDA reports)
FOETAL DISTRESS SYNDROME ( 5 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 5 FDA reports)
HEPATIC FAILURE ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
HODGKIN'S DISEASE ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
ACUTE HEPATIC FAILURE ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
BASAL CELL CARCINOMA ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
CACHEXIA ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
CONGENITAL NAEVUS ( 4 FDA reports)
COUGH ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DIAPHRAGMATIC APLASIA ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 4 FDA reports)
HYPOAESTHESIA FACIAL ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INTESTINAL PERFORATION ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 4 FDA reports)
MEDIASTINITIS ( 4 FDA reports)
MENINGISM ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
PLEURAL ADHESION ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
RENAL TUBULAR DISORDER ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
SKIN GRAFT ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
SUTURE RUPTURE ( 4 FDA reports)
THALAMIC INFARCTION ( 4 FDA reports)
TRISOMY 21 ( 4 FDA reports)
TUBERCULOSIS ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANAL PRURITUS ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
ASCITES ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CITROBACTER INFECTION ( 3 FDA reports)
COLOUR BLINDNESS ( 3 FDA reports)
DEFORMITY THORAX ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EXOMPHALOS ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 3 FDA reports)
HAMARTOMA ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
IMPATIENCE ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 3 FDA reports)
INJURY ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
KAPOSI'S SARCOMA ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LOSS OF LIBIDO ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OPTIC NERVE DISORDER ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PANCREATITIS CHRONIC ( 3 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 3 FDA reports)
PLACENTA PRAEVIA ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 3 FDA reports)
POLYDACTYLY ( 3 FDA reports)
PSOAS ABSCESS ( 3 FDA reports)
RENAL COLIC ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
SPASTIC PARAPLEGIA ( 3 FDA reports)
SPINAL CORD DISORDER ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
SUBACUTE COMBINED CORD DEGENERATION ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VERTIGO POSITIONAL ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VITAMIN B12 DEFICIENCY ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABSCESS NECK ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ALCOHOL ABUSE ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANORECTAL OPERATION ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
APATHY ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CELL DEATH ( 2 FDA reports)
CELL-MEDIATED IMMUNE DEFICIENCY ( 2 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 2 FDA reports)
CONGENITAL DIAPHRAGMATIC ANOMALY ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEFORMITY ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRY GANGRENE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ECHOGRAPHY ABNORMAL ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOETAL GROWTH RETARDATION ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GALLBLADDER OEDEMA ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HEAD CIRCUMFERENCE ABNORMAL ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
JAW CYST ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIPOATROPHY ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OESOPHAGEAL PAPILLOMA ( 2 FDA reports)
OSTEONECROSIS OF JAW ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PHYSICAL DISABILITY ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RECTAL TENESMUS ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TOXOPLASMOSIS ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHORIORETINITIS ( 1 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 1 FDA reports)
CONGENITAL SKIN DISORDER ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOETAL DEATH ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENITAL INFECTION ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GOUT ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOPULMONARY SYNDROME ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
HUMAN HERPES VIRUS 8 TEST POSITIVE ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INFERTILITY FEMALE ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYELONEPHRITIS CHRONIC ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL APLASIA ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
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SINUS BRADYCARDIA ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TAKAYASU'S ARTERITIS ( 1 FDA reports)
TESTIS CANCER ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRIFASCICULAR BLOCK ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VITRITIS ( 1 FDA reports)

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