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

DIARRHOEA ( 35 FDA reports)
PNEUMONIA ( 35 FDA reports)
DRUG INEFFECTIVE ( 31 FDA reports)
CONDITION AGGRAVATED ( 30 FDA reports)
ASTHENIA ( 26 FDA reports)
PYREXIA ( 25 FDA reports)
VOMITING ( 25 FDA reports)
FATIGUE ( 23 FDA reports)
NAUSEA ( 23 FDA reports)
DIALYSIS ( 21 FDA reports)
DEHYDRATION ( 20 FDA reports)
HAEMOGLOBIN DECREASED ( 20 FDA reports)
URINARY TRACT INFECTION ( 20 FDA reports)
DIZZINESS ( 18 FDA reports)
SEPSIS ( 18 FDA reports)
ABDOMINAL PAIN ( 16 FDA reports)
HEADACHE ( 16 FDA reports)
LOSS OF CONSCIOUSNESS ( 16 FDA reports)
MALAISE ( 16 FDA reports)
RENAL FAILURE ( 15 FDA reports)
RESPIRATORY FAILURE ( 15 FDA reports)
ATRIAL FIBRILLATION ( 14 FDA reports)
BRONCHITIS ( 14 FDA reports)
CONVULSION ( 14 FDA reports)
CROHN'S DISEASE ( 14 FDA reports)
HYPOTENSION ( 14 FDA reports)
RASH ( 14 FDA reports)
RENAL FAILURE ACUTE ( 14 FDA reports)
TREMOR ( 14 FDA reports)
DYSPNOEA ( 13 FDA reports)
SOMNOLENCE ( 13 FDA reports)
ANAEMIA ( 12 FDA reports)
ANOREXIA ( 12 FDA reports)
COUGH ( 12 FDA reports)
DISEASE PROGRESSION ( 12 FDA reports)
FEELING ABNORMAL ( 12 FDA reports)
INSOMNIA ( 12 FDA reports)
PAIN ( 12 FDA reports)
THROMBOCYTOPENIA ( 12 FDA reports)
WEIGHT DECREASED ( 12 FDA reports)
CHILLS ( 11 FDA reports)
FALL ( 11 FDA reports)
HEART RATE INCREASED ( 11 FDA reports)
HYPOAESTHESIA ( 11 FDA reports)
INFECTION ( 11 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 11 FDA reports)
ABDOMINAL DISTENSION ( 10 FDA reports)
BACTERIAL INFECTION ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
NEUROPATHY PERIPHERAL ( 10 FDA reports)
PANCYTOPENIA ( 10 FDA reports)
POST PROCEDURAL COMPLICATION ( 10 FDA reports)
RECTAL HAEMORRHAGE ( 10 FDA reports)
SINUSITIS ( 10 FDA reports)
ABNORMAL BEHAVIOUR ( 9 FDA reports)
ASTHMA ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
DRUG HYPERSENSITIVITY ( 9 FDA reports)
METRORRHAGIA ( 9 FDA reports)
CHONDROLYSIS ( 8 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
HYPERSENSITIVITY ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
MENTAL STATUS CHANGES ( 8 FDA reports)
MUSCLE SPASMS ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
ABDOMINAL DISCOMFORT ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
DIVERTICULITIS ( 7 FDA reports)
DRUG EFFECT DECREASED ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
HERPES ZOSTER ( 7 FDA reports)
MULTI-ORGAN FAILURE ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
NASOPHARYNGITIS ( 7 FDA reports)
NEUTROPENIA ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
PERITONITIS ( 7 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
STATUS EPILEPTICUS ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
DEATH ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DISEASE RECURRENCE ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
HAEMORRHAGE ( 6 FDA reports)
INFUSION RELATED REACTION ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
IRRITABLE BOWEL SYNDROME ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
SKIN ULCER ( 6 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
STRESS ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
ABSCESS ( 5 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
AGEUSIA ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
ARTHRITIS ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
BODY TEMPERATURE INCREASED ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CATHETER RELATED INFECTION ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
COLITIS ( 5 FDA reports)
CRYING ( 5 FDA reports)
CUSHINGOID ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
EAR PAIN ( 5 FDA reports)
ENTEROCUTANEOUS FISTULA ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
EXTRASYSTOLES ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
PENILE HAEMORRHAGE ( 5 FDA reports)
PEPTIC ULCER PERFORATION ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
RENAL TRANSPLANT ( 5 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
ANOSMIA ( 4 FDA reports)
APPENDICITIS ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CLOSTRIDIAL INFECTION ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
FAECAL INCONTINENCE ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HAEMORRHOIDS ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HYDROCELE ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
LOCALISED INFECTION ( 4 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
WOUND DEHISCENCE ( 4 FDA reports)
ABDOMINAL ABSCESS ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ALLERGY TO ANIMAL ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANAL FISTULA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
ASCITES ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BLAST CELL COUNT INCREASED ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD SODIUM INCREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BRAIN INJURY ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GASTROINTESTINAL PAIN ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
HYSTERECTOMY ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LISTLESS ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MUSCLE CRAMP ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
OTITIS EXTERNA ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
SEASONAL ALLERGY ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SLEEP TALKING ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
THROMBOCYTOSIS ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
WOUND ( 3 FDA reports)
ZYGOMYCOSIS ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ADHESION ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
ALOPECIA AREATA ( 2 FDA reports)
ALOPECIA EFFLUVIUM ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BONE INFARCTION ( 2 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CHORIOAMNIONITIS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 2 FDA reports)
COMA ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONGENITAL MEGAURETER ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
FUNISITIS ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GUN SHOT WOUND ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
IATROGENIC INFECTION ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTESTINAL STRANGULATION ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PARAPROTEINAEMIA ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PRECANCEROUS CELLS PRESENT ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL ISCHAEMIA ( 2 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
TONGUE ERUPTION ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABSCESS RUPTURE ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNION ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHOLINERGIC SYNDROME ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISTAL INTESTINAL OBSTRUCTION SYNDROME ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EAR TUBE INSERTION ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
EPENDYMITIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HUMAN IMMUNODEFICIENCY VIRUS TRANSMISSION ( 1 FDA reports)
HYDROCELE FEMALE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOKINESIA NEONATAL ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION SITE NECROSIS ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL CYST ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL STOMA COMPLICATION ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIGHT CHAIN DISEASE ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MASS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITOCHONDRIAL DNA MUTATION ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OVERCONFIDENCE ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIUMBILICAL ABSCESS ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINOPATHY OF PREMATURITY ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOTAL LUNG CAPACITY ABNORMAL ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
ULCER ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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