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

VIRAL LOAD INCREASED ( 68 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 57 FDA reports)
ABORTION SPONTANEOUS ( 54 FDA reports)
RENAL FAILURE ACUTE ( 50 FDA reports)
VOMITING ( 49 FDA reports)
DEPRESSION ( 47 FDA reports)
NAUSEA ( 47 FDA reports)
ANAEMIA ( 45 FDA reports)
DYSPNOEA ( 44 FDA reports)
RASH ( 43 FDA reports)
DRUG INEFFECTIVE ( 42 FDA reports)
DIARRHOEA ( 37 FDA reports)
INSOMNIA ( 37 FDA reports)
FATIGUE ( 36 FDA reports)
CHEST PAIN ( 34 FDA reports)
ABNORMAL DREAMS ( 31 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 27 FDA reports)
RENAL FAILURE ( 27 FDA reports)
THROMBOCYTOPENIA ( 27 FDA reports)
PYREXIA ( 26 FDA reports)
DIZZINESS ( 25 FDA reports)
DRUG RESISTANCE ( 25 FDA reports)
PREGNANCY ( 25 FDA reports)
MALAISE ( 23 FDA reports)
PRURITUS ( 23 FDA reports)
RHABDOMYOLYSIS ( 22 FDA reports)
APLASIA PURE RED CELL ( 21 FDA reports)
CARDIAC FAILURE ( 20 FDA reports)
CONFUSIONAL STATE ( 20 FDA reports)
CONVULSION ( 20 FDA reports)
LETHARGY ( 20 FDA reports)
PANCYTOPENIA ( 20 FDA reports)
ANXIETY ( 19 FDA reports)
ASTHENIA ( 19 FDA reports)
DRUG INTERACTION ( 19 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 19 FDA reports)
MEGAKARYOCYTES INCREASED ( 19 FDA reports)
BONE MARROW DISORDER ( 18 FDA reports)
DECREASED APPETITE ( 18 FDA reports)
HAEMOGLOBIN DECREASED ( 18 FDA reports)
LACTIC ACIDOSIS ( 18 FDA reports)
NEUTROPENIA ( 18 FDA reports)
RED BLOOD CELL ABNORMALITY ( 18 FDA reports)
STILLBIRTH ( 18 FDA reports)
WHITE BLOOD CELL DISORDER ( 18 FDA reports)
ABDOMINAL PAIN ( 17 FDA reports)
DEATH ( 17 FDA reports)
LOSS OF CONSCIOUSNESS ( 17 FDA reports)
CHOLESTASIS ( 16 FDA reports)
FEELING ABNORMAL ( 16 FDA reports)
HEADACHE ( 16 FDA reports)
HEPATIC FAILURE ( 16 FDA reports)
NIGHTMARE ( 16 FDA reports)
WEIGHT DECREASED ( 16 FDA reports)
ABORTION INDUCED ( 15 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 15 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 15 FDA reports)
NEPHROLITHIASIS ( 15 FDA reports)
PNEUMONIA ( 15 FDA reports)
RENAL TUBULAR DISORDER ( 15 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
COMPLETED SUICIDE ( 14 FDA reports)
CONGENITAL TERATOMA ( 14 FDA reports)
CYTOLYTIC HEPATITIS ( 14 FDA reports)
HEPATIC ENZYME INCREASED ( 14 FDA reports)
HIP DYSPLASIA ( 14 FDA reports)
MYOCARDIAL INFARCTION ( 14 FDA reports)
RASH MACULO-PAPULAR ( 14 FDA reports)
RENAL IMPAIRMENT ( 14 FDA reports)
SUICIDAL IDEATION ( 14 FDA reports)
PALPITATIONS ( 13 FDA reports)
PARANOIA ( 13 FDA reports)
ACUTE HEPATIC FAILURE ( 12 FDA reports)
BLOOD CREATININE INCREASED ( 12 FDA reports)
CRYPTORCHISM ( 12 FDA reports)
HYPERSENSITIVITY ( 12 FDA reports)
PAIN ( 12 FDA reports)
PARAESTHESIA ( 12 FDA reports)
TRANSAMINASES INCREASED ( 12 FDA reports)
DEHYDRATION ( 11 FDA reports)
HYDROCEPHALUS ( 11 FDA reports)
HYPOAESTHESIA ( 11 FDA reports)
RENAL TUBULAR NECROSIS ( 11 FDA reports)
CAESAREAN SECTION ( 10 FDA reports)
DISORIENTATION ( 10 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 10 FDA reports)
HAEMOLYTIC ANAEMIA ( 10 FDA reports)
MYALGIA ( 10 FDA reports)
PANCREATITIS ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
SEPTIC SHOCK ( 10 FDA reports)
SKIN EXFOLIATION ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
STEVENS-JOHNSON SYNDROME ( 10 FDA reports)
VISION BLURRED ( 10 FDA reports)
CONGENITAL CHOROID PLEXUS CYST ( 9 FDA reports)
COUGH ( 9 FDA reports)
FANCONI SYNDROME ACQUIRED ( 9 FDA reports)
HODGKIN'S DISEASE ( 9 FDA reports)
HYPERHIDROSIS ( 9 FDA reports)
LIVER DISORDER ( 9 FDA reports)
OSTEOPOROSIS ( 9 FDA reports)
RASH GENERALISED ( 9 FDA reports)
SUICIDE ATTEMPT ( 9 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 9 FDA reports)
ABDOMINAL PAIN UPPER ( 8 FDA reports)
ABNORMAL BEHAVIOUR ( 8 FDA reports)
ACROCHORDON ( 8 FDA reports)
ANGIOEDEMA ( 8 FDA reports)
DERMATITIS EXFOLIATIVE ( 8 FDA reports)
DYSPHAGIA ( 8 FDA reports)
FACE OEDEMA ( 8 FDA reports)
FLUSHING ( 8 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 8 FDA reports)
GYNAECOMASTIA ( 8 FDA reports)
HAEMATURIA ( 8 FDA reports)
HEART RATE IRREGULAR ( 8 FDA reports)
HEPATIC ENCEPHALOPATHY ( 8 FDA reports)
MENINGOMYELOCELE ( 8 FDA reports)
MENTAL DISORDER ( 8 FDA reports)
MOOD SWINGS ( 8 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 8 FDA reports)
PELVIC KIDNEY ( 8 FDA reports)
PREMATURE BABY ( 8 FDA reports)
RENAL DISORDER ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
SYNCOPE ( 8 FDA reports)
VERTIGO ( 8 FDA reports)
BACTERAEMIA ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 7 FDA reports)
DISTURBANCE IN ATTENTION ( 7 FDA reports)
DRUG LEVEL INCREASED ( 7 FDA reports)
DRY MOUTH ( 7 FDA reports)
FACIAL PARESIS ( 7 FDA reports)
FACTOR VIII INHIBITION ( 7 FDA reports)
HALLUCINATION ( 7 FDA reports)
HYPERKALAEMIA ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
LYMPHADENOPATHY ( 7 FDA reports)
MANIA ( 7 FDA reports)
MEMORY IMPAIRMENT ( 7 FDA reports)
MOTOR DYSFUNCTION ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
OSTEONECROSIS ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
PYELOCALIECTASIS ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
SLEEP DISORDER ( 7 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 7 FDA reports)
WOLF-HIRSCHHORN SYNDROME ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
AGGRESSION ( 6 FDA reports)
AGITATION ( 6 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
ANENCEPHALY ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
BURNING SENSATION ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
DYSGEUSIA ( 6 FDA reports)
GALLBLADDER DISORDER ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
HEPATOMEGALY ( 6 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 6 FDA reports)
LIVER TRANSPLANT ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
PRE-ECLAMPSIA ( 6 FDA reports)
RASH PRURITIC ( 6 FDA reports)
SKIN DISCOLOURATION ( 6 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ABORTION ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 5 FDA reports)
AGORAPHOBIA ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
BLOOD HIV RNA INCREASED ( 5 FDA reports)
BLOOD URINE PRESENT ( 5 FDA reports)
BRAIN NEOPLASM ( 5 FDA reports)
CATARACT ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CHROMATURIA ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
DEPRESSED MOOD ( 5 FDA reports)
DRUG DOSE OMISSION ( 5 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
ECTOPIC PREGNANCY ( 5 FDA reports)
ENTERITIS ( 5 FDA reports)
EYE DISORDER ( 5 FDA reports)
FAT REDISTRIBUTION ( 5 FDA reports)
GASTROINTESTINAL TOXICITY ( 5 FDA reports)
GENERALISED ERYTHEMA ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HEPATIC CIRRHOSIS ( 5 FDA reports)
HEPATITIS FULMINANT ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
INTRA-UTERINE DEATH ( 5 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
PERSONALITY CHANGE ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
RENAL COLIC ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
ABSCESS LIMB ( 4 FDA reports)
ADENOMA BENIGN ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ANGER ( 4 FDA reports)
ASCITES ( 4 FDA reports)
BILE DUCT OBSTRUCTION ( 4 FDA reports)
BIPOLAR DISORDER ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
BURNING SENSATION MUCOSAL ( 4 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
FALL ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
GENOTYPE DRUG RESISTANCE TEST POSITIVE ( 4 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
KLINEFELTER'S SYNDROME ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 4 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 4 FDA reports)
NECROSIS ( 4 FDA reports)
NORMAL NEWBORN ( 4 FDA reports)
OSTEOPENIA ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 4 FDA reports)
PELVIC MASS ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 4 FDA reports)
RENAL PAIN ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 4 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 4 FDA reports)
SALIVARY GLAND CALCULUS ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SPINA BIFIDA ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TREATMENT FAILURE ( 4 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABSCESS ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
APHASIA ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BILIARY DYSKINESIA ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
BURKITT'S LYMPHOMA ( 3 FDA reports)
CELL DEATH ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
CONGENITAL ACROCHORDON ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CRYSTAL URINE PRESENT ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DIABETES INSIPIDUS ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
ENANTHEMA ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FOETAL ALCOHOL SYNDROME ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
IMPATIENCE ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LIVE BIRTH ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
MENINGOCELE ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NECROTISING RETINITIS ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OESOPHAGEAL INJURY ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
OSTEOPOROTIC FRACTURE ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
PRENATAL SCREENING TEST ABNORMAL ( 3 FDA reports)
PRODUCT COUNTERFEIT ( 3 FDA reports)
PRODUCT LABEL ON WRONG PRODUCT ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RENAL TUBULAR ACIDOSIS ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SLUGGISHNESS ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
TOOTH HYPOPLASIA ( 3 FDA reports)
TRIGEMINAL NEURALGIA ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
VASCULITIS GASTROINTESTINAL ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VIRAL MUTATION IDENTIFIED ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ALOPECIA AREATA ( 2 FDA reports)
ALOPECIA TOTALIS ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
AMNIOCENTESIS ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COMA ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ENDODONTIC PROCEDURE ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FATTY LIVER ALCOHOLIC ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOPITUITARISM ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INTRAUTERINE INFECTION ( 2 FDA reports)
IRITIS ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
MALARIA ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENSTRUATION DELAYED ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MICTURITION FREQUENCY DECREASED ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUCOSAL ULCERATION ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MYELOID MATURATION ARREST ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEURAL TUBE DEFECT ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLACENTA PRAEVIA ( 2 FDA reports)
PREMATURE DELIVERY ( 2 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SIALOADENITIS ( 2 FDA reports)
SIGMOIDECTOMY ( 2 FDA reports)
SIGMOIDITIS ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TABLET ISSUE ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THERMOHYPERAESTHESIA ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
TOOTH EROSION ( 2 FDA reports)
TOOTH REPAIR ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALOPECIA UNIVERSALIS ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANTIVIRAL DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ASTHENOSPERMIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BINGE DRINKING ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CRYSTALLURIA ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHILIC PUSTULAR FOLLICULITIS ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOETAL ARRHYTHMIA ( 1 FDA reports)
FOETAL DEATH ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC HYPERMOTILITY ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPROTEINAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KAWASAKI'S DISEASE ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACROPHAGES INCREASED ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROSYPHILIS ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRESENILE DEMENTIA ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY TUBERCULOMA ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
SALMONELLA SEPSIS ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHIGELLA INFECTION ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN MALFORMATION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TERATOSPERMIA ( 1 FDA reports)
TETANY ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TRANSFERRIN DECREASED ( 1 FDA reports)
TRANSIENT PSYCHOSIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
ULCER ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UNWANTED PREGNANCY ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VIROLOGIC FAILURE ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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