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

PYREXIA ( 133 FDA reports)
VOMITING ( 120 FDA reports)
HEPATITIS ACUTE ( 114 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 99 FDA reports)
CHOLELITHIASIS ( 98 FDA reports)
BLOOD PRESSURE INCREASED ( 58 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 49 FDA reports)
LUNG ADENOCARCINOMA ( 33 FDA reports)
HEADACHE ( 32 FDA reports)
DYSPNOEA ( 29 FDA reports)
INFUSION RELATED REACTION ( 29 FDA reports)
ARTHRALGIA ( 28 FDA reports)
NERVOUSNESS ( 22 FDA reports)
NASOPHARYNGITIS ( 21 FDA reports)
RHINORRHOEA ( 20 FDA reports)
DIZZINESS ( 19 FDA reports)
LIVER DISORDER ( 18 FDA reports)
PRURITUS ( 18 FDA reports)
RASH ( 18 FDA reports)
CHEST PAIN ( 17 FDA reports)
CHILLS ( 17 FDA reports)
COMPLETED SUICIDE ( 17 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 17 FDA reports)
DRUG INEFFECTIVE ( 16 FDA reports)
URTICARIA ( 16 FDA reports)
SOMNOLENCE ( 15 FDA reports)
ANXIETY ( 14 FDA reports)
ASTHMA ( 14 FDA reports)
CROHN'S DISEASE ( 13 FDA reports)
DEATH ( 13 FDA reports)
TACHYCARDIA ( 13 FDA reports)
FATIGUE ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
PNEUMONIA ( 12 FDA reports)
COUGH ( 11 FDA reports)
FEELING ABNORMAL ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
PARAESTHESIA ( 11 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 11 FDA reports)
ARRHYTHMIA ( 10 FDA reports)
HYPERSENSITIVITY ( 10 FDA reports)
HYPOAESTHESIA ( 10 FDA reports)
UNRESPONSIVE TO STIMULI ( 10 FDA reports)
BACK PAIN ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
MALAISE ( 9 FDA reports)
PAIN ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
TREMOR ( 9 FDA reports)
ARTHRITIS ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
MALABSORPTION ( 8 FDA reports)
MUSCLE SPASMS ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
SUBILEUS ( 8 FDA reports)
ASTHENIA ( 7 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
DRUG DOSE OMISSION ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
INJECTION SITE PAIN ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
PREMATURE BABY ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
ANAPHYLACTIC SHOCK ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
BASAL CELL CARCINOMA ( 6 FDA reports)
BRONCHITIS ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
CONTUSION ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
MIGRAINE ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
PRODUCT QUALITY ISSUE ( 6 FDA reports)
SUICIDAL IDEATION ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
VISUAL IMPAIRMENT ( 6 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
DRY MOUTH ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HEPATIC FAILURE ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
EYE INFLAMMATION ( 4 FDA reports)
FALL ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
LOCAL SWELLING ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 4 FDA reports)
PEMPHIGUS ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
PURPURA ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYPOPNOEA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INJECTION SITE IRRITATION ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LIBIDO DECREASED ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MIDDLE INSOMNIA ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
APATHY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CERVICOBRACHIAL SYNDROME ( 2 FDA reports)
CHLOASMA ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DEVICE LEAKAGE ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DREAMY STATE ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
EYES SUNKEN ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LEUKAEMOID REACTION ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEDULLOBLASTOMA ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL NEOPLASM ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLACENTAL TRANSFUSION SYNDROME ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RETCHING ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
THOUGHT INSERTION ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
URETERIC OPERATION ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VOCAL CORD PARALYSIS ( 2 FDA reports)
VULVAL ULCERATION ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTI FACTOR XI ANTIBODY POSITIVE ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR XI LEVEL DECREASED ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONGENITAL ADRENAL GLAND HYPOPLASIA ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIAPEDESIS ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOPHILIA ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL OEDEMA ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SCHISTOSOMA TEST POSITIVE ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC MASTOCYTOSIS ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THYMUS HYPERTROPHY ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TIC ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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